QIAGEN NV Stock

All right. Good afternoon, everyone. I'm Robby Bamberger, senior research analyst covering life sciences and diagnostics here at Baird. We're pleased to welcome QIAGEN this afternoon. Especially pleased to welcome Jon Pratt, who became QIAGEN's CEO on September 1. So we're catching him right at the 2-week mark. We also have Roland Sackers, QIAGEN's CFO and Domenica from IR with us as well. Thank you guys for all making the trip.

Jon, just before we get into the business, I wanted to start with you. You stepped into the CEO seat September 1, so we're catching you 2 weeks in. What was it about QIAGEN that made you want this job? And in your conversation with the Supervisory Board, what were they telling you they wanted most for the next CEO of QIAGEN?

Yes. Thank you again. Good to be here. I guess I knew QIAGEN. I've been involved in the space through Pall and through Beckman Coulter and through Waters for a long time. I knew QIAGEN from an undergrad perspective. Almost every customer I touched was the blue boxes, so to speak. And so I knew the brand, did a bit of research on the brand and in terms of the customer intimacy and the quality of the people employed in QIAGEN, it was a pretty exciting place to come. So I was intrigued to join. It took a long time because I was in the business of selling Filtration Group to Parker Hannifin. So there was a long transition period. So it gave me a chance to understand the company a lot.

Supervisory Board, they really felt that they obviously wanted the industry experience, allied experience. In no particular order, they were pleased that I lived and worked in the U.S. and U.K. As you can tell from my accent, I was not exactly born in Brooklyn. So that fitted well. They wanted somebody that could bring some simplicity, shall we say, to some complexity, strategic focus very much execution-driven. My experience with Waters and others was an execution kind of game in many, many ways. So all the things aligned well there. Somebody that would fit with the culture. So lots and lots of things.

And you spent most of your career in businesses that looked a lot like QIAGEN, President, Beckman Coulter Life Sciences, inside Danaher, senior roles at Pall and then the Waters division at Waters Corp. So what are the maybe 1 or 2 things from those seats that you think could travel best to QIAGEN?

I think the 2 things I'd highlight is R&D effectiveness, choice, prioritization linked to strategy. They're very much part of the Waters and Pall journey. And then the other one is, I would say, commercial execution in all its forms. Beckman and Waters in particular, we benefited from upgrading kind of the commercial capabilities. The depth of technical capability is always there, but commercial execution in all its forms is something I would say that was important.

And then now how are you spending your first 90 days? And then when should investors expect to hear your view on the strategy and medium-term framework for QIAGEN?

Yes. Obviously, listen-learn phase, right, diving deep. I had quite a bit of time pre-appointment to dive deep, but building on that, getting to know the enterprise, the people, the places. I have been traveling to all of our facilities, really trying to understand how we win in each of our growth pillars and what the midterm outlook is of that, and frankly, where we probably should double down on and where we should manage differently. So classic onboarding process really.

Yes. And Roland, I'll include you on this one. The strategic review of the company, framed it as a continuous process with 3 paths, continue organically, strategic partner or a financially driven partner. So can you maybe walk through all of those 3 options from your seat now?

I don't think that I want to distinguish between the different parts of it. But I do think it's very fair to say, and Jon, I think, was alluding to that right now, there's clearly a path A and there's a path -- plan B. And again, we will -- one thing is also very clear, we want to have rather a clear direction rather sooner than later. It's nothing what we want to decide end of this year or whatever. Of course, we need a clear path going forward. And I think we are all very much committed to that and delivering on that. Again, right now, by definition, I can't give you much more update other than that we're working hard to get rather in weeks than in months to a clear decision.

That makes sense. And maybe diving into specific segments, starting with diagnostics, which is your in vitro diagnostic test you sell into hospital and labs. The segment was down 2% constant currency in Q2, improving from 4% last quarter, down 4%. The big piece inside of it is QuantiFERON, 25% of revenue, the blood test for latent TB. Given lower immigration testing expectations, you took out $35 million from revenue, which is essentially all of your U.S. exposure. So maybe 2 quarters into that impact, where do we stand on immigration volumes? And you took that essentially 100% of U.S. immigration testing exposure out. Does that still look like the right call? Or is that -- is some of that coming back? How are you thinking about that?

Good question. Just a slight adjustment. So we took out $35 million, that's correct, but $30 million U.S., $5 million Middle East, where I do believe that the $5 million -- or we do believe the $5 million Middle East over time will come back because I'm quite sure that, that is an area where we probably will see either the war stops or they find a way to go back into routine work. As you know, it's particularly about construction workers working coming from some countries and work in this environment.

And yes, I do believe or we do believe the $30 million probably will be out for quite some time because the legal immigration laws in this country have changed, and I don't think there's any cation that -- any indication that they change any quite soon. Nevertheless, I think it's also important to recognize that, that is going to annualize more or less February next year. So we should see that, that is fading away as a quite significant headwind.

And then maybe taking out aside immigration, what did the remaining 90% piece of QuantiFERON grow this quarter? And what are the drivers? And essentially, is that the right jumping point for 2027 as we look forward?

Again, if you do the math and just adjust for that apples-to-apples, that clearly leaves you in the kind of somewhere between 5% and 7% growth rate. So I think that is probably also compared to the market growth, which is 4% to 5%, probably a good assumption. So I would say, overall, over time, that is also the way we look at the business. As I said, immigration most likely will not come back. If it comes back, we are ready. I don't think that's going to happen.

At the same time, that is the most important message about QuantiFERON. It is still a 50% to 60% skin test market, so 120-year-old skin test, which still has a majority of the overall share, and the overall market is growing 4% to 5%. So there's a lot of room for us to expand in the market. We're clearly the #1 player in that market, and therefore, we continue to gain share.

And just confirming the immigration comp should essentially be end of Q4, so Q1 should be a clean quarter?

I would say February is the first month, which is clean.

Okay. And then for competition for QuantiFERON, who are the new entrants that you're competing against there? And which geographies? Have you had a chance to change like price or contract terms to defend any of your accounts? Or is it pretty still -- pretty much the leader there?

One thing we always have to remind the market on is QuantiFERON was always competitive, right? Again, while we have significant market share, there was always players and there was always a Revvity, there was always a bioMérieux. There's always a handful of Asian players. So it's not always -- yes, we are clearly the leading player, but we are not the only player.

Now of course, there's another player, most likely over time, entering the European market. Again, there's no sign right now that, that is happening to the U.S., might happen, again, as they're saying, beyond '27. If that is '28 or '29, time will tell. But, of course, we haven't stand still, right? We clearly were very actively in working with our customers in long-term contracts. We have now close to 60% of our contracts of our customers in long-term multiyear contracts.

Again, we did a lot, and you have seen that around automation, the Inpeco solution will come end of '27 to the market, which is the only one fully walkaway workflow automation available in the market. So I do think we have a very strong setup. And of course, we can talk about some details of the competitive environment in terms of testing, but we feel quite comfortable.

And you've been building on new patient populations just beyond traditional health care worker screening, immunocompromised patients, diabetics, now dialysis. So can you maybe just frame how large those new populations are and how much of them are actually in numbers today and which are still left to grow?

So it's a smaller part compared to the rest of testing groups like health care workers and so on. But it's the fastest-growing piece of the target groups that we're looking at. Yes. So that's basically what we're working on also to get more patient groups into the QuantiFERON test. And -- yes.

Just to enhance on that a bit, quite about 10% of our overall IGRA QuantiFERON test is immunocompromised patients. That is also by far the fastest-growing patient group. It is also -- again, there's a lot of talk about incoming competition. This is actually one of the areas where they're struggling because to address that perfectly right, you have to have a CD4, CD8 test. We do have that. Others don't have that.

Yes. So would you say the biggest of those other populations would be immunocompromised patients?

Right now, yes. Over time, of course, diabetes, as you know, is an attractive market opportunity because there's clearly a lot of patients around that and a lot of potential. There's a clear correlation between them. And again, getting into latent TB, it's probably a bit more out, but it's clearly on the watch list of some of the health care standard setters.

The fully automated Inpeco workflow and the AI risk scoring tool, those land in the second half of 2027. When do those actually become revenue for you? And then, how should we -- how do you expect to monetize them?

The monetization starts more or less as early as in '27 because at the end of the day, it is a huge opportunity, particularly for midsized to larger labs to have walkaway solution. Have in mind, QuantiFERON is also for our customers, one of the largest revenue generation they have in the lab. And having that in a -- and again, the walkaway solution is a significant step up. It's one of the limitation factors they're all having. And so we are looking forward to that as our customers are.

And maybe let's move to QIAstat-Dx, your syndromic testing platform. Growth was 7% in Q2 after down 1% constant FX in Q1. You're guiding to low double digits in the second half of the year. I guess, what's driving that recovery in H2 versus H1 besides a little bit of easing comps?

In all fairness, H1 was untypical for QIAstat because we were clearly -- actually also the whole industry fighting very strong respiratory sales in H1 last year, right? So on a more normalized basis for the second part of the year, we also expect that it returns to significant growth rate, most likely even double digit.

On top of that, we were able to continue our portfolio expansion. You have seen that we brought BCID to the market. The next one is critical urine infections. So I would say both are still going quite well, placements of new instruments, but also portfolio build-out. Again, that we had a strong respiratory season last year was good news for last year, but you know it is, right? It makes it -- it doesn't make your life easier in the following year.

And is there any assumptions that you embed in for the flu season for the second half of the year?

As you know, we like that you all do these big conferences because it is at the end of the day very helpful for us. But joking aside, I do think right now, the tendency looking into Australia and U.S. is probably a more regular or softer environment.

Got it. And the blood culture panels are the most interesting new menu addition that you have. And you said you're confident of FDA approval by year-end. Can you maybe frame the size of that opportunity? What the realistic 2027 contribution looks like there?

It's a bit early to size it. But of course, they are important factors to the portfolio. Again, respiratory is and will be always the leading panel. Nevertheless, it makes it unique, and it makes the reason why customers choose your platform, and I do think that is important. As you know, my favorite term is always a bit like an espresso machine, right? We all like to have an espresso machine, and we all like that they have 20 different flavors. At the end of the day, we all typically buy the 2 or 3 we use the most, but having the choice is what differentiates it. And I think that's exactly the case here as well.

Great. And kind of moving on to Sample Technologies, which is your front end of every molecular test, the instruments and kits that essentially pull DNA and RNA out of the blood before anything gets analyzed. Sample Technologies, it grew 9% this past quarter and Q1 as well. Organic was about 3%, excluding Parse. And you've guided to double-digit growth in H2 on a reported basis. So can you maybe just walk us -- walk through what gets us to that low double digit from 9% the last couple of quarters?

Yes. I mean, we -- I have the privilege of walking into an instrument replacement cycle. We've got 3 new instruments from the highest throughput, which we typically didn't compete in a very, very high throughput right through now to the Mini, which is a benchtop instrument for individual scientists. I think price points south of $10,000, simplifying an individual scientist workflow. There's 100,000 of those opportunities to install that and enjoy the revenue from that as well. So those launches are here and now. The Mini is launching pretty much as we sit here. So that's creating some momentum in the back half as well.

Yes. And then automated consumables, that grew high teens. How much of that base is automated versus manual now? And then, how should we think about that conversion from just manual to automated over time?

Majority is clearly still manual. But as you know, we on purpose drive conversion to automation because at the end of the day, it is a trend. In every lab, you have an increase in volume, but you have less people available in front of to do the work. So I do think automation is a significant part of the solution.

And second, of course, there's only very few companies like QIAGEN, and we are clearly by far the leading player in providing this different automation level, as Jon was referring to it, on the low level and the mid-throughput level, but also in the high throughput level, which is quite new for QIAGEN. So we do believe there is a significant automation opportunity. And you have seen that, right? If you go back to the last 3 quarters, we have seen already a step-up in underlying growth for sample prep, but we're still in the early days. So I do think there's more opportunities for us going forward.

And you now have 2 of the 3 new sample prep systems in the market with QIAmini still to launch. You sized them at about $20 million of incremental H2 revenue. Does that still seem about right? And how is the placement funnel building there?

The good news is today is September 15. That means the Mini is launched as well. So we have all 3 machines -- we have all 3 machines in the market, which is great news. So there's no launch risk. Actually -- but you're right, we are a couple of weeks early. So your numbers were right. It's good that we are early, which is also good. No, we feel comfortable.

Again, clearly, we are -- I think it's also fair to say we are not living in the easiest capital expenditure environment, particularly in the U.S. So we always have to balance that, and we have to see what the next couple of weeks and months are bringing. Some people are talking about budget flushes or not. That is a discussion we can have. Some people saying, okay, let's see what the results are in the midterms that might ease up a bit of the confidence issues, some people having. So I do think overall, there's opportunities for us, which might add on.

And then how many QIAsprint Connect systems have been placed? And then, how is the initial feedback that you're getting so far?

By definition, I'm not going to tell you how many we placed so far. But I think it's fair to say that our goal for this year is that we have around 150 systems in the market, and we feel good about that.

Yes. The only thing I'd add to that is I talked very briefly about commercial execution and building that muscle in QIAGEN. It's a perfect time to do that with 3 new instruments into the core of the business in sample prep, a complete portfolio there and 100,000 new opportunities for the Mini, it fits really well into our commercial execution program. So no comment on the 150, but you can guess where I think that should go.

Yes. That's helpful. And what's the consumable pull-through per placement when you have that QIAsprint Connect? And how long until a new box is pulling through at that mature rate?

Again, it's a bit early days, but I think we clearly said that this is a high throughput market opportunity, and there is a big market opportunity. And as you know, we have -- while we are for sure and nobody will disagree with that is the leading player in sample preparation, we have never had, for certain reasons, played in the high throughput area. There's an area where, for example, there's 10,000 KingFisher machines in the market, right? Most of them are 5 to 10 years old. So there's a significant opportunity for replacement.

QIAsprint is a new generation. It's a generational shift machine in terms of pull-through, in terms of time to result in one force, all the new features you have to have, continuous load and random access, fully automated and integrated in your LIMS system. So we do believe the machine will make a difference, and therefore, should generate quite significant pull-through in that.

I mean, we're sizing it. It's critical to commercial execution because that's total cost of ownership as you have it. But I would say this, these are the kind of instruments that generate kind of their own revenue value in a full year when they're fully operational. So it's very much a revenue stream. That's why placements are absolutely critical. And if you think about the price of a unit when it's fully operational, fully running, it's delivering that in annuities plus service, so consumables plus service as you go forward.

And then Sample Tech instrument revenue growth was up mid-single digits in Q2. How much of the sample prep instrument strength is new launches versus underlying replacement demand?

It's a mix. Again, we are just still very early, this new placement, as we said before, Mini is just starting more or less this week. So again, we do believe there is clearly more contribution coming over time from the new ones. Nevertheless, overall, sample prep automation also had a good start into the year, right? As you know, we have different types of machines, cubes and so on. So overall, again, we are quite happy with the environment. Again, good academic market being a bit more stable? Absolutely.

Yes. And Jon, are you -- is there anything you're bringing in, in terms of like the sales motion to sell new instruments at all from your past positions?

Yes. It reminds me very similarly of journeys at Beckman and Waters. Instrument placement -- instrument replacement cycle being very structured in the way you approach your replacement cycles. When you talk about a new launch, there's 3 possibilities: you displace a competitor, you upgrade your instruments upon cycle and that cycle we're working through. But think 5 years-ish, you think about new instrument cycle. And then there's greenfield, if you like, new placements. The Mini is very much a new placement. The others have those other opportunities as well. That's all part of the -- right from demand generation to sale. That's all something that we installed in those enterprises. And it's exact parallel with the razor-razor blade here at QIAGEN.

Great. And Parse, good acquisition, tracking above $40 million you set for the year. I guess, what's driving that upside versus your initial $40 million expectation?

As you said, it's going quite well, starting the year with $40 million, probably more now, more than $45 million. I think there's 2 main reasons right now. One is, as you know, we have compared to others in the field, an automation instrumentation-free solution, which, again, given what we discussed on CapEx environment is clearly a plus. And second, which is as meaningful is we clearly have a different -- and that's the reason why you do acquisitions, right? We have a significant footprint also with biopharma customers. And therefore, I think bringing just Parse much closer into this kind of environment helped us to secure quite a good number of contracts.

And the liquid biopsy prep, that grew more than 30% in 2025. You noted Natera, Guardant, NeoGenomics as key customers. So how large is that piece now? How does volume growth at those customers then flow straight to you guys?

So it's a smaller part of our Sample Tech, but it's an important part. You can also see it with the launch of the QIAsymphony Connect that is specifically optimized for liquid biopsy customers dealing with different volumes that they're handling, and liquid biopsy samples are very tricky. So you need to have the highest quality possible, and that's what we provide with our kits and with our automation. So it's for us a focus. And whenever our customers -- and keep in mind that those customers are relying on a good sample preparation. Without the sample preparation, you can forget about the rest. And this is basically what we offer. And when they are growing nicely, then it's also good for us, and we're happy about that.

That's great. And moving to PCR and nucleic acid amplification, you described the shift from being a PCR company to being a digital PCR company. How far through that transition are you?

I'm not referring to American sports because I'm still here, but you would probably say we're not even in the first inning or I believe that's very early. No, I guess, it's early days. qPCR, as we all know, is a $2.7 billion market opportunity. Digital PCR, if you look at all players in the market, are probably around, I don't know, $500 million, $600 million. So there's a lot of way to go, and both markets, of course, growing quite nicely.

Just to reiterate what I said before, we had a great start into this year, give -- more or less close to 20% in Q1, close to 20% in Q2. I don't think the second half will be much different. And that in an environment where capital expenditures is still quite difficult, right? So pull-through is adding nicely up.

I think we did a great job in really expanding menu. We always had the outstanding machines. I think nobody has questioned that. But for quite some time, we were a bit under par in terms of portfolio. That has changed more or less this last year. So we still continue to expand menu. I think it's paying off quite nicely.

And then how does the margin profile differ between digital PCR versus traditional PCR?

I would -- both are good. No question. Again, both are, I would say, CFO's darling. And actually, it's true for both. It is for instrumentation and consumables, where sometimes instrumentation, it can be a bit more challenging. But here, we have both instruments, very healthy margins.

That's great. Maybe moving just to end markets, academic and government, you said research funding improved in Q2 versus Q1. What are you assuming for academic growth into the second half, flat or continued improvement there?

I would say our assumption is right now that we have, I would say, an underlying positive impression of the market development, but we do not believe there's any significant uplift. I would really defer that to '27 when we have more insight how stable the NIH budget, in particular the discussions around that.

Have in mind, we are in a quite -- I wouldn't say a unique situation because it happens from time to time. But the money is actually being distributed. It's about get -- does the money get spended. And that is the confidence, which is much more emotional and where we need stability. And I do think that is something that it's hard to influence for a company. It is really something what happens on the larger scale.

Yes. And then pharma, biotech, how is overall bio -- pharma and biotech showing up in your order book? And is there a way to sort of parse out between early stage and later stage pharma, biotech?

It's clearly an area where a lot of things are happening, right? And AI, for example, is a big topic in that environment right now, and you have seen some of our announcement in general. I think it's also here, it's moving in the right direction. It's not the single biggest part of our business, but clearly with some momentum.

Yes. And then regionally, Americas turned positive this last quarter. EMEA was negative. I guess, what drove that reversal? And what are you guys assuming also for China from here going on?

Starting with the latest one. China for us is around 4% of total. So compared to other companies, I would say it's not as meaningful. We also see a slight improvement in China, but slight improvement means less negative in all fairness. So I would -- the good news for us here is we have a quite strong second brand in China. You might recall that's quite unique to QIAGEN that in China, we have not only the global QIAGEN brand, but 2005, we actually acquired our single largest copycat and always kept it separate, own management, own R&D, own production. And we clearly can see the difference between the Chinese brand in China and the global brand. And I do think that helps us to hedge some of the impacts, particularly also U.S. company seeing.

And then on financials, tariff refund, you noted $0.02 EPS benefit for the year is already in the outlook with anything more being incremental. Can you maybe walk through the mechanics and timing of those tariff refunds?

Yes. First of all, the $0.02 is net of customer refunds. So it's one thing. We'll see how quickly the U.S. Treasury Department pays us, but we are quite sure that happens this year. And if it will be a bit more, even better. Let's see how it goes.

And then maybe just thinking about the pace of guidance through Q3 and Q4. Q3 is expected to grow 1% to 2% constant FX and then growth is expected to accelerate into Q4. Can you maybe just size that step up? How much of that acceleration is the comp on government shutdown and then also just overall sequential demand?

Yes. Good question. Thanks for that. It's an important question as well. And I guess, you gave part of the answer already by yourself. Have in mind, the difference is actually not too much between Q3 and Q4 apples-to-apples because last year, 2 of the 3 months was a shutdown literally in U.S., so there's clearly a certain impact from the prior year.

The second is also what we discussed, and I think Jon was alluding to, we feel quite comfortable on the new product launches right now. Again, it's not only sample prep, it's also sample prep. We have the same thing what we discussed on QIAcuity, same thing what we discussed on QIAstat. And we have still a lot of other business where we launch new products. So we do believe the new product, particularly also the instrumentation placements goes quite well. That will more or less close the gap of $5 million to $10 million to the step-up. I'm quite sure that is not a bigger deal for us.

We have about a minute left. Would you maybe just cap off what are your 2 biggest opportunities for the next year, 2 or 3, whatever?

Yes. So I mean, I think I've alluded to it, right? Organic growth focus, commercial excellence in all its forms. I think there's a pricing opportunity that we haven't talked much about. That's very real. I think our sample prep, instrumentation renewal, similarly on QIAcuity as well and then our menu expansion on QIAstat. At the end of the day, that's about executing on those products that were all introduced this year. So that's priority A as we go into the new year.

And of course, we've got to refine the strategy a little bit of the company. We're going through a process. We'll probably have a Markets Day at some point, I think spring/summertime when we refine that. So those would be my 2 focuses for now.

Do you want to add anything to that?

Perfectly said.

Awesome. That's about all the time we have. So with that, please thank Jon, Roland, Domenica for the conversation, and I appreciate you guys for coming.

Thank you very much. Appreciate it.

Thanks for having us.

Thank you. Cheers.

All right. Welcome, everyone, to our fireside chat with QIAGEN. I'm Aisyah Noor, Head of European MedTech Research at Morgan Stanley. It's my pleasure to host QIAGEN's CEO, Jonathan Pratt, and CFO, Roland Sackers today, as well as IR, Domenica Martorana. Before we start, I'm obligated to inform you to check ms.com/researchdisclosures for important disclosures and to check with your MS sales rep if you have any questions.

With that, welcome, John and Roland. It's great to have you here in New York. And Jonathan, for the first time as CEO of QIAGEN, very pleased to have you. If we kick off with your recent joining of QIAGEN, it's great that you've decided to join us here today. Could you briefly introduce yourself and why you decided to join this organization? And what do you see as the biggest opportunities in this business?

Okay. Well, thank you, Aisyah. Hello, everyone. Good to be here. Briefly introduce myself. As you can probably tell by the accent, I'm a Brit. I grew up in Europe, moved to the States in '01. In the industry, I was -- I spent a lot of my career at Pall Corporation, where I ran their laboratory businesses, some of the instrumentation businesses and their food and beverage businesses. From Pall, I ran as President of Beckman Coulter Life Sciences as part of Danaher and did that for a few years, moved to Florida in the process.

After Beckman Coulter Life Sciences, I led what we call the Waters division at Waters Corporation, which was about 90% of the corporation at that time. And from Waters, I actually took an opportunity to run Filtration Group, which was a life science process tech and industrial enterprise that we were going to take public. But as it happened, we had strategic interest and sold that company -- about -- we closed it about 2 weeks ago, 2.5 weeks ago, I would -- the QIAGEN Board had approached me to join earlier in the year, and we eventually were able to join as CEO 2 weeks ago.

The next part of your question was what attracted me to QIAGEN?

Yes.

So I guess the first thing to say is I'm a scientist. I'm an undergrad chemist. I first used QIAGEN in the lab. And from there, in each of my career steps, the kind of ever-present QIAGEN blue boxes were in the labs, be it in Waters, be it in Pall Corporation, Beckman, et cetera. So I knew the brand. I knew the reputation of the brand, which was pretty much deep customer intimacy and high-quality product. When I joined, I was intrigued, so went to speak to the Board. And then the portfolio itself is very interesting. In Sample Prep, we touch kind of every part of the health care space. And so we're exposed to everything in Sample Prep, and it's a kind of deep-rooted part of the organization. The recent interesting acquisitions and bolt-ons in NGS. We also have the digital PCR franchise as well as the recent Parse acquisition. And also there's a diagnostic play, which each of the niche kind of two stools. You've got the QIAstat and QuantiFERON. So interesting portfolio.

And then you look at that and say, what can I bring to it? If there's been a theme in my career, it's been simplifying the complex, capital allocation focused on 1 or 2 things, not 6 or 7 things. It's kind of a theme. And then bringing that right down through an enterprise in terms of choice and simplicity sounds easy, but it's kind of what I tend to try and bring to it from a strategic choice perspective, make sure you're structured to execute on that strategic choice. But I'm a front-end guy really, a commercial guy. I think if there's a theme again through Beckman and Waters and others, it's improving that commercial execution, really bringing commercial excellence, sales funnel management, demand generation, product launch excellence, everything through a business. And in a business like ours, which I love because it's razor or razor blades, every single placement matters, every single instrument matters. And so having a great front-end commercial enterprise can really serve you very, very well. So I thought I could bring a lot of that to it as well. And so here I am with QIAGEN.

If you think about your principles as a CEO, what do you consider the most important priorities for an organization, public listed? Is it top-line growth, profitability, EPS growth, free cash flow returns? Help us think about that.

Yes. At the end of the day, in the situation we're in QIAGEN right now, I think growth is a priority. We have some sensible margin expansion opportunities as well. And I think some of those comes from wonderful things like price and growth and instrument choice, et cetera. Roland, perhaps you want to comment on where you see QIAGEN from a capital allocation perspective right now?

No. I think -- as you know, we have since 2012, I would say, a long-standing capital allocation policy. First and foremost, we're happy to invest in organic growth opportunities. I'm quite sure that also our focus on bolt-on acquisitions is still there. I don't think that we're looking for anything larger in terms of transformative deals. But of course, we do have excess cash. And if there's an opportunity once we more or less continue to have excess cash and the current net debt to EBITDA, as you know, is below 1, there's opportunity also to continue with share buybacks. Most important is we ask on the latest AGM for the approval. So if the Board decides to move forward, we can do it at any time.

Yes. I'd add as well. In terms of bolt-on acquisition, we'd do something tomorrow if it made sense. But I think strengthening the core, strengthening our execution, being the best owner of an asset comes from how strong you execute in many ways as well. So I think there's a lot of focus on bringing into it on organic execution as well.

Okay. Excellent. I wanted to start the discussion around AI. You recently announced an AI partnership in testing with the QIAsymphony Connect. Just talk us through the AI-driven automation opportunity and any benefits you see or hoping to see in your kind of early tests?

Yes. No, I think you're referring to the [ Anthropic ] design topic because, again, together with the MHS part of the business, I think there's a very nice opportunity for QIAGEN to extend its standardization even in the days of AI -- at the end of the day, it is about automation of our instruments in a lab environment. It's about standardization. It's about early detection of troubleshooting. There's more and more workflows in all labs from research all the way to clinical where you have -- which are very data-rich. And of course, having here an opportunity to being early stage involved, again, that is just one part that's more to come, makes a difference. We started here with QIAsymphony. There's for sure an opportunity to go left and right.

Okay. Would this -- if you think about the software integration layer used to monitor the QIAsymphony Connect today, would this be applicable across your fleet of the sample tech instrumentation? And could you talk about the use cases or customer types that make most sense to adopt these automation layers? And when do you see that translating into a financial opportunity?

Just to remind everybody, we have more than 30,000 sample prep machines out there. So there's a lot of opportunities for us as well for our customers. I do think it makes sense for large-scale customers because like as I said, there's a lot of data generated and of course, workflow automation, LIMS embeddedness is key to them. But even in smaller settings, having walkaway solution, having opportunities to control that even if you're not in the environment, makes a significant opportunities, having automation being stand-alone operated.

So I don't think there's any specific limit to the size of our customers nor to the kind of origin of a customer, if it's a clinical environment, a research or a pharma company. We're seeing interest coming from all different groups. Again, we're early stage in a research preview. Nevertheless, I do think given the speed of AI in these days, there's an opportunity to get that hopefully in some way out next year.

Okay. And in terms of use cases, what types of applications are you seeing AI being used today beyond this you mentioned troubleshooting. What types of comments of in a pharma, are you having those discussions with the biopharma customers at the moment? Or is it academia?

As you know, we have a lot of different areas where AI is already embedded into our revenue streams. First and foremost, clearly, all our QDI solutions have an integrated AI part because at the end of the day, everything is what comes out of the sequencer has a significant data size. But the same is also true for QIAcuity, for example, because at the end of the day, also here, it's a quite data-rich process and qualification and validation is an important part of that. And AI, again, plays an -- or can play even a more important role going forward as well.

But that is only the one part of the business. There's another offering which comes around QuantiFERON. We talked about that, enabling our customers or the health care providers at the end of the day with the interpretation of the data is somebody going from latent to active TB, where you see on this path. We are the only company having this hundreds of millions of different data points, which enables the interpretation.

But AI, of course, is not only something what we do on the revenue side. We do it also in-house, think on operations. We have AI embedded validation processes, for example, for identifying scrapping, if you talk about QIAstat. AI plays an important role for us if it comes, for example, to customer care, first-level support, more than 50% of all answers in the meantime, getting AI answered on the first level. So there's a lot of opportunities for us. QIAGEN has more than 300 software developers in the company, quite sure that they're all looking forward that their life gets easier, more effective using this kind of tools. AI is changing also our world.

Yes. Perfect. Okay. If we take it back to kind of 2026 and 2027, if we look at -- start with the sample tech business. So the organic growth per your guide is going to accelerate for sample tech quite significantly in the second half. How confident are you in achieving this? And how much of that is pricing versus volume? We know you're launching some new products, Connect, Mini. Can you provide some KPIs on how that's gone so far?

First and foremost, we have seen already -- this is starting this year, a nice underlying acceleration of the sample prep business. We have now, I think, the third quarter in a row with a 3% growth rate ex Parse, which again speaks for itself. Parse, of course, is on top. We were very clear that Parse when we moved into the year, we were expecting around $40 million in revenues. Right now, we are rather at $45-plus million. So it's moving in the right direction.

On the organic business, I would say also here, the pipeline is building quite nicely. The good news is QIAmini is now also in the market a few days earlier than we thought, which is always good news. And we're quite, I would say, optimistic on that contribution going forward. Nevertheless, it's also fair to say the overall academic market, while improving in the U.S., is clearly not in a normal environment, right? It is clearly something where still confidence building has to happen. Nobody knows what the next weeks bring in terms of election results on which -- whatever kind of communication from any politician might change. So there's a lot of factors which we can't control. Nevertheless, on the product side, we believe it goes in the right direction in terms of placements, but also in terms of consumables.

Okay. Just on the U.S. academic and government segment specifically, how is the academic budget spend trending so far by your estimates? The NIH data would suggest there is money flowing in, but it's not being spent. What do you think the customers need to see to start investing into R&D once again?

Caution is the word I would use. It's improving, but slowly. And you're right, there seems to be a disconnect between available funds and spend. It is very slow to ramp. I think in the U.S., you've got some midterms coming up. And whilst they won't have any direct impact, I think there's a confidence factor that may come from results depending on how those midterms go, it be in the U.S. and all that. So I think there's just a sense of what's next.

And so there's a little bit of caution on spend. Does that result in some sort of end-of-year flush? We haven't factored that in, so to speak. But I think the midterms will play even emotional component on the way money is being spent at the moment. Some of the instruments we're launching like the Mini, for example, will probably have no real impact on that in a good or negative way because the price is a capital point that tends to be a bit more of a fast spend rather than a true capital spend. So we've got some offsets to that depending on that. But I think fundamentally, the midterms will have some emotional effect.

Okay. We touched on the Parse acquisition currently. It's -- is this business being impacted by the current weak market conditions or the Middle East disruption? And can you size the midterm growth opportunity here for Parse?

I'll start by saying I'll hand it to Roland and I start saying the Parse is ahead of plan as we head through this year.

Yes. And just also to frame it a bit in terms of numbers, '24 was $20 million in revenues, as we said, '26, probably, let's say, $45 million plus. So you can see the acceleration, and we're quite sure that we will continue to see that. The current environment might be somewhat helpful for Parse because as you know it is automation-free. So again, it's for sure, a nice alternative. Clearly, a good benefit is that now being able to integrate Parse also in our pharma sales force, which by factor is larger than what Parse had as a stand-alone company is being quite helpful. So a lot of success in pharma right now from Parse comes out of the biopharma connection, and we do not see any reason why that should change. So we're also very optimistic looking now into '27.

Okay. Maybe a last one on your launches in QIA -- in sample tech, specifically the Mini, the Connect and the Symphony. Where are you at in the ramp and sales contribution for those products? Are we just at the early innings? Or are you halfway through? Just kind of talk through that?

It's just at the early innings. I'll start by that. Roland can add some color. And we haven't really launched the Mini yet, so that there's really no material revenue at all from that. Having said that, the Mini has hundreds of thousands of potential placement opportunities. So you will see a ramp from it. But on the others, I'd say it's fairly early stage. You see a little bit of it in the back half, but it's really a 2027 ramp. The sales funnels are growing, building stronger, but it's really early innings. Any other color?

F

Yes, I'm not good in U.S. sports so big, Jon. But nevertheless, just compare with QIAsymphony, right? We sell QIAsymphony in 2008. So you clearly see it, it takes some time. Nevertheless, the pipeline is filling quite nicely. I think we are -- again, right now, we are well on track.

I'm not very good at U.S. sports either, so I think -- we're at lunch on the second day of the cricket test for anybody that's interested in that analogy.

Okay. If we move on to QuantiFERON. So how is the U.S. latent tuberculosis testing market trending versus your expectations? Is the immigration destock that we saw earlier in the year fully behind us? Just give us some color there.

Yes. Just to remind everybody, what we said earlier this year is that the $50 million global immigration testing market or for TB testing clearly was seeing some changes. $30 million of that is U.S. -- was U.S.-based. And with the change in immigration laws in the U.S., we more or less have seen this business collapsing at the end of the day. And we also do not believe that it comes anytime soon back because the policies and immigration in the U.S. probably will stay as it is. In particular, legal immigration, it's legal immigration. It's only very true, very small part about illegal immigration, we believe -- we don't believe that it goes back to the levels we have seen before.

$5 million we took out, which was related to the Middle East TB testing. Here, we do believe that is probably coming back over time because quite sure either the war there stops or we will see any other kind of opportunities that these areas go back into a more normalized environment because there's a lot of construction going on, a lot of people from whatever Pakistan, Bangladesh, India working in this environment. And once they go back, they have to get tested again. So that is rather a question of time.

Now ex immigration, I think there's a general understanding that the overall market is growing somewhere between 4% and 5%. There's no reason that, that is going to change. Skin test is still the majority of the overall market, somewhere between 50% and 60% of the global latent TB testing is still the literally 120-year-old skin test. There's an ongoing penetration that should benefit QIAGEN going forward.

Okay. Perfect. And then with respect to Roche TB competition, we know this product is now in the European market. U.S. market launch is TBD, although rumors say it's a few years out from now. Have you seen any signs of competition or customer preferences post Roche's launch in Europe?

I think there, nothing really has changed. I think there was clearly, I would say, a good set of clarity provided on the Roche Capital Market Day about their product. I think there was a good education done about what are clearly some of the workflow issues they're going to face. Just to remind everybody, it's quite obvious that they can't cover CD4, CD8. It's quite obvious in the meantime that they do have a requirement for refrigeration step in between. And it's also quite obvious looking on their own documentation that the indeterminate rate is by factor of 5 higher than ours, which means 1 in 20 patients has to come for retesting. Actually even [indiscernible] has to be reblooded, which is a significant topic for any kind of lab. If you have labs with 100,000 and plus tests per year, having this kind of magnitude to be again reblooded is an important topic. So I would say there was quite some education coming out of that. It's still too early to see what it means for the European market because they are just starting it.

Okay. And with respect to -- you have a high throughput product for QuantiFERON coming out in the coming years. Could you remind us what segment of the market this device is going to -- or this product is going to serve? And what portion of your total sales could see a benefit from this product launch?

If you're talking about the Inpeco automation, which probably comes out by end of '27. So it's a quite decent future. First and foremost, a fully automated workflow available for latent TB, which I do think is important, particularly for a segment, I would probably call it mid-throughput to higher throughput. So very large labs typically also invested in their own automations. Again, there's a lot of documentation available, for example, what Quest did around the QIAGEN automation solution a couple of -- actually 2 CMDs ago. They featured it quite prominent on their own Capital Market Day. So I would argue there is a significant group in between which loves to get this walkaway solutions.

Okay. Moving on then to QIAstat. It's been quite a bumpy ride for a lot of respiratory multiplex sales providers this year given the lower flu testing dynamics. What are your assumptions for the intensity of the flu season this year, given Australia data has been trending weak and CDC data doesn't show much signs of improvement either?

It depends what you call improvement. But I've seen a pretty normalized flu season, not a particular peak flu season. Roland?

Yes. I'm always glad that a lot of analysts following the flu seasons around the world. Again, our assumption is rather a normal environment. Last year, as we all know, the first half of the year, we had a very strong flu season. That was the reason why we had also clearly a significant headwind this year. We do believe that rather in the second half of the year, we are back to double-digit growth rate for QIAstat. And I do think that is probably the better way to look at that business.

Okay. And with respect to QIAstat competition, have you seen any signs of more aggressive pricing from competitors like DiaSorin? Have you seen the third-generation GeneXpert platform launched by Cepheid in ADLM? Do you think that could present a more credible competition in the U.S. market?

I'll say on the Cepheid product, it's limited on its multiplexing that's probably 10 or 11. So it's not in the same category, but commentary on competition beyond that?

I don't think the competition has in any way changed since more or less the last 2, 3 years. At the end of the day, it's 2 parties and which is bioMerieux and us. The others are around, but I wouldn't say not even close to be as visible. If you look at Cepheid, for example, again, the GI panel has, I think, different pathogens. It's not even half of what we are having and what the industry standard is. So they might catching up, but not anywhere close. The strength of the QIAstat was anyway the automation, the cartridge, the ease of use that is still unparalleled in the whole industry.

You've launched for QIAstat several non-respiratory panels in the U.S. in recent years like gastrointestinal, meningitis, blood culture. How are these helping the placement trends? Are you winning share? And if so, who from?

So it's always good to have a broad menu. We started with the core 3 panels, which is respiratory, GI and meningitis. And I think I need to steal this example from you, Roland, the Nespresso machine, right? Usually, you have only a couple of flavors that you like and that you regularly use. But of course, the more flavors, the more attractive the platform. And that's basically what we're focusing on to add menu. We added 2 blood culture panels in Europe and also 1 in the U.S., 1 more to come by the end of this year. And that's basically how we are completing our menu or extending our menu.

Complicated UTI is going to be a key differentiator for us because we would be the very first one offering a syndromic panel on complicated UTI and also a pneumonia panel is in our pipeline. The other thing is also QIAstat is able to do qualitative and quantitative detection, which also opens up the companion diagnostics field for the QIAstat, and we have 3 partnerships on that running and also continue to build that pipeline.

Okay. Now moving on to QIAcuity and digital PCR. So this end market has also seen a slowdown in parallel with the weaker trading environment in the first half. How is your platform performing versus competitors like Bio-Rad, in particular, given their last PCR acquisition?

It's always a definition of slowing, but I think we are now 2 quarters with more or less close to 20% growth rate. So we're quite happy with that. Nevertheless, it's a fair comment, Aisyah, that, of course, the last 2 years were very difficult, as we talked about for capital expenditures, and that was clearly also affecting digital PCR. Nevertheless, therefore, we are even more excited that things getting again more normal. We are not 100% normal, but more in a normal direction. But what is driving growth right now, a very fair observation is clearly generating pull-through.

If you go back now over the last few years, I would say it was always quite obvious that QIAGEN had the better workflow, the better machines. It hasn't really changed. But for clearly some time, we had a smaller menu. There was clearly other companies or one other company who had a broader menu. But I do think we closed that gap quite nicely. We pushed very hard last year to have hundreds of additional panels and assays out there. This year is even probably -- again, probably more than 1,000 additions. So there is a significant menu expansion. So that gap is closed, and that helps us right now quite nicely.

Okay. Perfect. And then moving on to QDI or QIAGEN Digital Insights. How is the license to SaaS subscription transition progressing? And could this still persist as a headwind in 2027?

Just to remind everybody, historically, QIAGEN was typically signing 3-year plus license agreements with pharma company. So just by definition, if that goes into SaaS, it is a 3-year cycle before you have worked through that. Now using your U.S. sport, we're probably in the last innings somewhat, but we still have to go through it. So that's probably where we are. I hope that the overall AI momentum also will help us to get at least to high single digit and hopefully soon back to double digit. Do I go to promise that today for next year? Absolutely not. But is it the right business to be in? Absolutely, yes.

Okay. Okay. And then moving on to margins. Can you run through the cost inflation and tariff headwinds you expect to impact the margin this year? And how should we think about how this evolves as you go into 2027 versus your more than 31% margin target by 2028?

Yes. First and foremost, let me remind everybody that we will end this year probably with an EBIT margin, again, north of 29%, probably constant exchange rate, 29.5%. If I compare that apples-to-apples with our CMD of 2024 target of for '28 with 31%, we're actually going to meet it this year already. Why? Because when we have given the Capital Market Day, the 100 basis points dilution from Parse was not in it. The 150 basis points tariff headwind was not in it, and there's clearly also a bit on FX. So we are already literally apples-to-apples with 31% for this year. Doesn't mean that I'm telling you today, now we are done, we are finished? Absolutely not. We're going to continue to improve our margins. We have this what we call QIA efficiency program. It has 40 different efficiency programs, initiatives within the company, we're going to continue with that. And there's, I think, a clearly laid out plan for further margin improvement.

Take tariffs, for example, right? While it is a relative hit for us, clearly, we were able to protect EPS actually to a larger degree. Why? Because we were more or less sharing the pain with our customers. But of course, if you pay 50 and you get reimbursed 50 by your customers, the margin is still relatively 0, but EPS outcome is still quite well protected.

Okay. Could you maybe just talk through the main cost headwinds that you're seeing right now, which buckets that you're seeing kind of inflationary headwinds, so whether it's freight, plastics, metals, anything like that and where you're seeing most kind of pain, I guess?

Inflation in general is a topic. Nevertheless, and I'm quite sure that with Jon now for having an increased focus around pricing and seeing opportunities there that might be probably become even a tailwind for us at some point in time. But also so far, we were able to -- given our overall gross margin structure to protect our margin in that regard. Like any other company in our industry, roughly half plus of our costs are headcount related. So inflation is a topic.

Yes. And on the price side, the more and more instruments we sell, the sticky nature of our solutions and our consumables. Yes, pretty openly internally and externally said that we certainly have pricing opportunity, and it's a commercial negotiation skill contract by contract, but I think we can certainly offset that going into '27 quite comfortably.

Okay. All right. Moving on to buyback and capital allocation then. So you've announced a mega buyback this year with 10% of share capital and then $200 million on top. When could you start executing on this?

We announced that we have -- the Board has the right to do so. The good thing shareholders approve that. Again, there was clearly some time we had to wait, which is more or less in these days over. So technically, there is an opportunity to go into the market. There's clearly a couple of other factors we have to embed in that decision. Again, there's clearly enough publications around that there's a strategic review going on in QIAGEN. So probably nobody expects during such a time frame, any kind of share buyback going to happen.

But the good news is we do have the flexibility to do a regular share buyback. We still also can do another $200 million synthetic share buyback, which is very much favored from particular retail shareholders and European shareholders. So I think there's enough opportunities for us to do so. And as I said, in terms of net debt to EBITDA, we also feel very comfortable around that.

Okay. And then on M&A. So you've been quite consistent with the M&A pipeline, almost 1 bolt-on every year since I started covering QIAGEN, which is great and the most recent one being Parse. So you're generating about $0.5 billion in free cash flow a year. So technically, even with the buyback program, you still have some optionality left. So what interests you in the market? And where do you see white spaces in your portfolio?

I can answer that quite clearly. I'm not going to obviously name targets, but I'm still getting my teeth into the areas of interest, shall we call it, acquisition vectors. And that fits in with the strategy choices, right? Can we simplify the enterprise? Can we focus our attention in 2 areas, not 5. So I think that entire areas under review. Of course, there are targets in pipeline. And if the right acquisition was available tomorrow, we can make that acquisition.

Okay. And then I would love if you could address the elephant in the room with respect to the M&A headlines that have been there for QIAGEN this past year without commenting on the rumors directly. Just talk through the pros and cons of QIAGEN operating as a stand-alone business and whether it would make more sense to leverage the resources and scale of a larger entity in the market.

I think you're asking the question that's with the Supervisory Board right now is what is the long-term future. I think it's important color to add from my seat. I agreed to join QIAGEN early in this year. We just had to wait a while until we could close the other transaction and I could join the company. And so this recent strategic review was as a late fly into my equation. I came here to build QIAGEN as a stand-alone. I think it's important to know that our plan A is that. And then subject to any strategic review of the Board, it is a finite strategic review, and we're talking weeks rather than months as to whether where we can conclude where we are with that. But of course, we're still traded. So what means closed. But yes, all I'd say is the process is running in the background. I'm not personally involved in it. I'm here for plan A to build QIAGEN. Pros and cons, I'll leave that for the others, if you want to comment on it.

Okay. That takes us to the end of the session. Jon, Roland, Domenica, thanks so much for the insights today. And to the audience, thanks for participating. Thank you, everyone.

Thank you for the question.

Thank you.

Ladies and gentlemen, thank you for standing by. I am Shelly, your global meet operator. Welcome, and thank you for joining Qiagen's Q2 2026 Earnings Conference Call webcast. [Operator Instructions] Please be advised that the call is being recorded at Qiagen's request and will be made available on the Internet website. [Operator Instructions]

At this time, I would like to introduce your host, Daniel Wendorff, Vice President, Head of Investor Relations at Qiagen. Please go ahead.

Thank you, operator, and welcome to our call for the second quarter of 2026. We appreciate your time and interest in Qiagen. Joining the call today are Thierry Bernard, our Chief Executive Officer; and Roland Sackers, our Chief Financial Officer. Also joining us is Dr. Domenica Martorana from our Investor Relations team.

As always, today's call is being webcast live and will be archived in the Investor Relations section of our website at www.qiagen.com, where you can find the press release and presentation accompanying this call. Please also note that this call will include forward-looking statements. Actual results may differ materially from those projected due to a number of factors outlined in our most recent Form 20-F and other filings with the U.S. Securities and Exchange Commission. We will also refer to certain financial measures not prepared in accordance with U.S. generally accepted accounting principles or GAAP, that provide additional insights into our performance. Reconciliations to the most directly comparable GAAP figures are in the release and presentation. All references to earnings per share refer to adjusted diluted EPS.

With that, let me hand over the call to you -- let me hand over the call to you, Thierry.

Thank you, Daniel. Hello, and good morning, good afternoon or good evening, depending on where you are in the world, and thank you for joining us. Let me start by thanking again our teams across Qiagen for their continued dedication and disciplined execution. Their focus enabled us to deliver results above our outlook while continuing to invest in our portfolio and focus on profitable growth.

Let me now walk you through our key messages for today. First, we exceeded our outlook for both sales and adjusted EPS. Net sales were $535 million and unchanged on both a reported basis and at CER. This was ahead of our outlook for an approximately 2% decline CER. Adjusted diluted EPS was $0.62 on both a reported basis and at CER again, above our outlook of at least $0.60 at CER. Those results demonstrate the resilience of our business and provide further confidence in our outlook for the year.

Second key message, our growth pillars delivered 5% growth at CER, profitably above market growth. Sample Technologies led the quarter, reflecting continued demand for our sample preparation solutions. QIAcuity delivered another solid quarter, driven by healthy consumables demand. QDI, our bioinformatics business also performed well, led by our clinical application. QuantiFERON returned to growth as solid demand across many testing groups more than offset the significant decline in U.S. immigration testing demand. This U.S. immigration testing demand decrease is what we highlighted at the end of our Q1 2026.

QIAstat Diagnostic was impacted by a challenging prior year comparison in respiratory testing, partially offset by continued strong growth in our gastrointestinal and meningitis/encephalitis panels with the gastrointestinal panel performing particularly well. Third key message, we maintain a very high level of profitability. This reflects our ability to improve efficiency while continuing to invest for future growth. Fourth, we continue to generate strong cash flow, providing the financial flexibility to invest in the business while returning capital to shareholders. This financial strength enabled us to increase our annual dividend by 40% in 2026. And this brings me to my final key message for today, our outlook for 2026.

We are reaffirming our full year outlook and remain confident in stronger growth during the second half of the year. The continued performance of our growth pillars and the progress we are making across our portfolio reinforce our confidence in delivering the outlook we have set for the year.

With that, I'll turn over to Roland for more details on the financials.

Thank you, Thierry, and hello, everyone. As Thierry highlighted, we delivered a better-than-expected second quarter, exceeding our outlook for both sales and adjusted diluted EPS while maintaining a high level of profitability. Let me start with our sales performance across the 4 product groups.

Sample Technologies rose 9% CER, driven by automated consumables and higher instrument sales compared to the year ago period. Diagnostic solutions declined 2% at CER. QuantiFERON returned to growth at 1% CER as solid demand across most testing groups more than offset reduced immigration testing demand, primarily in the U.S. and Middle East. QIAstat-Dx sales declined 7% at constant exchange rates despite growth in GI and meningitis panels.

However, this was more than offset by lower respiratory panel sales against a challenging prior year comparison previously communicated. In PCR and nucleic acid amplification, sales declined 8% at CER. Our digital PCR system, QIAcuity, delivered double-digit growth at CER, driven by strong consumables demand. This is more than offset by weaker OEM demand.

[Technical Difficulty]

[Operator Instructions] You may continue.

Okay. Sorry for that. It looks like we had some technical difficulties, but I do think we are now back on a call. So let me continue.

In PCR and nucleic acid amplifications, sales declined 8% at CER. Our digital PCR system, QIAcuity, delivered double-digit growth at CER, driven by strong consumables demand. This was more than offset by weaker OEM demand. In the genomics and NGS product group, sales rose 2% CER. Qiagen Digital Insights delivered solid single-digit growth, while consumables for universal NGS panels used on third-party sequencers grew more than 20% CER.

Lower sales of other genomics products moderated the overall growth rate. Regional performance was mixed during the quarter. Sales in the Americas rose 1% CER, led by 2% growth in North America, while sales declined in Brazil and Mexico. In the EMEA region, sales declined 2% CER. While Spain, Belgium and Poland were up in the quarter, Germany, France and Italy were down. In the Asia Pacific region, sales declined 2% CER. Excluding China, the region grew at a low single-digit rate at constant exchange rates, supported by high teens growth in Japan, while China was down in the low teens.

Sequentially, sales in China improved at a double-digit percentage rate. Moving down the income statement. Profitability remained at a high level. Adjusted operating income declined 2% and reached USD 157 million. The adjusted operating income margin was 29.4% compared with 29.9% in the second quarter of '25. Disciplined cost management and efficiency gains helped offset gross margin headwinds. The adjusted gross margin was 66.2% in the quarter compared with 66.7% in the prior year period due to changes in product mix.

Operating expenses remained broadly stable as a percentage of sales. Sequentially, the adjusted operating income margin increased by 200 basis points from 27.4% in the first quarter of '26 with higher operating leverage contributing to the improvement. Adjusted diluted EPS was $0.62 at constant exchange rates, exceeding the outlook of at least $0.60 at CER. The adjusted tax rate was 18% in the quarter, in line with our target of 17% to 18%. The high level of profitability also translated into solid cash generation.

Operating cash flow was $301 million for the first 6 months of '26, unchanged from the same period of '25. This was achieved despite approximately $20 million of cash payments for efficiency and restructuring programs and a planned increase in inventory. Cash generation was supported by disciplined working capital management and a higher level of profitability. Improved receivables collection and other working capital movements helped offset the inventory build. Days sales outstanding improved to approximately 55 days from approximately 57 days at the end of '25.

Days inventory outstanding increased to 153 days from 149 days at the end of '25, reflecting inventory build in preparation for new product launches. Our high level of profitability and cash generation continues to support a strong balance sheet. This gives us the flexibility to invest in innovation, pursue targeted acquisitions and return capital to shareholders. In line with this approach, we completed a $500 million synthetic share repurchase in January and paid our second annual dividend of around $72 million in July. The dividend per share increased by 40% to $0.35 from $0.25 in '25.

With that, let me hand back the call to Thierry.

Thank you, Roland. And let me now highlight some of the recent progress of our teams in our portfolio. Let's start with Sample Technologies. We continue to make good progress with our automation strategy as more laboratories transition from manual to automated sample preparation. With the commercial launch of QIAsymphony Connect, our new IVD compliant automation system, we reached another important milestone in expanding our automation portfolio. We have started also placing QIAsprint Connect and are pleased with the number of placements, the high level of customer acceptance and the very positive initial feedback, especially from pharma company.

QIAmini, our third launch for this year, remains on track for launch this fall with beta field testing beginning in North America in the coming weeks. We are also making very good progress in single cell analysis with Parse. We recently launched the next generation of immune profiling solutions, further expanding our single cell offering. Parse was also selected for a NASA supported research program aboard the International Space Station, supporting research into new treatments for cartilage injuries.

Together, those developments show how we are broadening our portfolio while enabling new areas of research in latent tuberculosis testing. As latent tuberculosis screening continues to expand, laboratories are looking for more efficient ways to manage growing testing volumes. Together with DiaSorin and our new automation partner, Inpeco, we plan to launch the first fully automated Sample to Insight workflow in the second half of 2027. This combines sample handling, incubation and detection into one purpose-built automated workflow for QuantiFERON testing.

We are also developing an AI-enabled tool to help assess the risk of progression to active TB, providing clinicians with additional insights beyond the detection of latent TB infections. This is how we continue to innovate around QuantiFERON, creating additional value for laboratories and clinicians. On QIAstat, we continue to expand the menu into new testing areas. Bloodstream infections require rapid treatment decisions. With the launch of our 2 new BCID panels, QIAstat now expands into bloodstream infection testing in Europe, providing laboratories with broad coverage across relevant pathogens and antimicrobial resistance markers. Together, those 2 panels detect 33 pathogens and 28 antimicrobial resistance markers in about 1 hour time to result.

The next step is to bring those panels to the U.S., and we are confident to get our FDA approval by the end of the year. We are also seeing the value of menu expansion for QIAstat in the field. An example is that during the ongoing cyclospora outbreak in the U.S., our large gastrointestinal panel is helping laboratories respond to increasing testing demand. Turning to digital PCR and QIAcuity now. We continue to advance digital PCR across research, biopharma and clinical application. As more customers are moving from qPCR to digital PCR, they are looking for workflows that are scalable, automated and easy to standardize. This is why we continue to expand the QIAcuity portfolio.

This year, in the second half of the year, we are launching new gene expression assays together with a high multiplex kit for the analysis of up to 12 RNA targets in a single reaction. We are also expanding our cell and gene therapy offering with new software and broader workflow automation through our collaboration with Hamilton. We recently demonstrated again the flexibility of QIAcuity during the recent Ebola outbreak, where we rapidly introduced custom digital PCR assays to support infectious disease research and surveillance.

Finally, let me touch on Qiagen digital insights development. AI is becoming increasingly important in biomedical research as researchers work with growing amounts of data, but AI is only as valuable as the scientific knowledge behind it. This is where QDI, Qiagen Digital Insights comes in. We combined more than 25 years of curated biomedical knowledge with AI to turn complex biological data into meaningful insights. We, for example, recently announced a new collaboration with NVIDIA. Together, we are combining our curated biomedical knowledge with accelerated computing and graph-based AI. This will help researchers all over the world accelerating drug discovery.

With that, let me hand it back to Roland with the details of our outlook for the second half of the year.

Thank you, Thierry. Let me now provide an update on our outlook for '26 and the third quarter. For the full year, we are reaffirming our outlook for total net sales growth of about 1 to 2 percentage points at CER. We also continue to expect adjusted diluted EPS of at least $2.43 at CER. For the third quarter, we expect total net sales growth of about 1% to 2% CER and adjusted diluted EPS of at least $0.62 at CER.

I would like to give you some additional perspectives on the expected performance in the second half of the year. We expect CER sales growth to improve from minus 1% in the first half to about 3% to 4% in the second half. This represents a sequential improvement of approximately 4 to 5 percentage points. There are 3 main drivers behind this development. First, the end of the year-on-year headwinds from the discontinued NeuMoDx and DIALUNOX portfolio is expected to contribute approximately 2 percentage points to the improvement in the second half.

Second, we expect approximately another 2 percentage points from increasing contributions from new Sample tech systems and other recent and planned product launches. This include QIAsymphony Connect and QIAsprint Connect in Sample Technologies. The rollout of our new BCID panels and continued momentum in companion diagnostics for QIAstat-Dx and additional offerings for QIAcuity. As mentioned earlier, QuantiFERON delivered a stronger second quarter. We continue to believe that we are tracking towards our $500 million target for '26 with easier comparisons expected to support performance in the fourth quarter.

Third, we expect approximately 0.5 percentage point from the combined benefits of Parse, which is performing ahead of our original '26 sales target of about USD 40 million and modestly improving trends in the U.S. life science environment. Within the second half, growth is expected to be weighted towards the fourth quarter, which benefits from the incremental contributions from the previously mentioned product launches and an easier prior year comparison following the disruption caused by the U.S. government shutdown in the fourth quarter of '25.

The expected allocation towards the second half is also consistent with our historical sales phasing. Approximately 47% of our full year sales are generated in the first half and approximately 53% in the second half of the year. On the topic of tariff repayments, we foresee for the full year. Net of customer refunds, this could be a benefit of about $0.02 EPS at CER. This is already included in our outlook and any additional benefit would be incremental also to our guidance.

Finally, let me briefly address currency trends. For the full year, we currently expect a tailwind of about 1 percentage point on sales and a neutral impact on adjusted diluted EPS. This is unchanged from our previous assumptions. For Q3, currency is expected to have a negative impact of about 1 percentage point on net sales, but be neutral on adjusted diluted EPS.

With that, I'll now hand it back to Thierry.

Thank you, Roland. And now let me briefly summarize before we move to the Q&A session. First, we delivered a quarter above our outlook for both sales and adjusted EPS. At the same time, we maintained a high level of profitability while continuing to invest in our portfolio. Our growth pillars continue to perform well, delivering above-market growth, led by Sample Tech, QIAcuity and QDI, while QuantiFERON returned to growth. We are making good progress in our product launches, supporting our growth ambition for the second half of the year and beyond.

Together, the performance of our growth pillars and the progresses on new launches reinforce our confidence in a stronger second half of 2026. So in closing, we remain focused on achieving the outlook we have set for this year and delivering solid profitable growth.

With that, I would now like to hand back to the operator for the Q&A session. Thanks a lot once again for your attention.

[Operator Instructions] We will now take the first question comes from your line of Casey Woodring with JPMorgan.

Maybe just walk through the updated guide for us. I think the back half, you took down from 4% to 3% to 4%. Just maybe walk through kind of what's changed? And then any sort of seasonality that you're assuming from 3Q to 4Q, the step-up that you talked about a little bit Roland in 4Q. Maybe just walk us through the drivers there.

Thanks, Casey. I can take the first half of your question and in Roland's comments, we described also the weight of H2 and the traditional seasonality beyond Q4. But -- so first of all, we believe in that acceleration for the reasons that we highlighted. And by the way, we also highlighted the same reason in our Q1 release. You have obviously some positive impact coming from the stop of headwinds coming from the discontinuation last year of NeuMoDx and DIALUNOX. And we expected -- we expect also a significant input from our new launches, especially in Sample tech, but also the new panel that we described today for QIAstat.

But at the same time, we want to remain cautious. There is no doubt in our view, Casey, that, for example, funding, especially in the U.S., is improving sequentially. We see indeed an improved funding, especially for research and academia in Q2 compared to Q1. At the same time, we need to highlight that if you consider, for example, the funding coming from NIH in the U.S., it is still below in H1 of 2026 compared to H1 2025. So we see improvement, but we remain also cautious because, as you know, the lack of funding sometimes reflects on capital sales and abilities from labs to invest into new instruments.

At the same time, we will benefit definitely from an easier comp from Q4 '25 compared to Q4 '26. Remember that last year, we started the year quite strong in Q1 '25 at 7% growth. We finished the year in Q4 '25 at 1% growth. This is why we have an easier comp.

Roland, do you want to give more details on the weight of the different quarters?

Yes. And probably a couple of different perspectives. First of all, just on some of the products, right? What we just described, Casey is, again, you heard that sample prep is doing quite well, improving quarter-over-quarter. We had now in the first half, 9% growth rate. Again, that will move double digit in the second half of the year, right? QIAstat, we just talked about that for the first half, there was clearly a significant headwind coming from the respiratory business last year.

We do believe that business also, again, will turn probably high single, more likely low double-digit growth rate as well in the second half of the year. QIAcuity is probably even accelerating while it's already high double digit in Q1 -- sorry, in H1. So I think there's a lot of things where we, I would say, also have reasonable visibility in a given market environment. So I would say there's things like that. But one thing to you mentioned it before, that is one thing this product launches, right? It takes some time that they gain traction, sample prep, you see it. But of course, every quarter, having instruments on the market, customers getting used to that is being helpful.

There is, I think, the natural reason that the fourth quarter will be a stronger one. And have in mind also QIAmini is going to hit within the third quarter, the market. So there's clearly also contribution coming in the first quarter as well.

We'll now take your next question coming from the line of Jack Meehan with Oberon Research.

For Thierry. So you've announced the strategic review and still have the CEO search going on. I was wondering how should we view the status of the strategic review when a new CEO is named? Does that mean the review stopped? Or could that continue as a separate topic? Any thoughts would be great.

Yes. So I think you need to consider that those are 2 complementary but also independent processes. The CEO search, obviously, is one of the highest duty of the Board. We are progressing. We confirm that the transition will happen in H2 of 2026. But at the same time, we have always outlined that our company is always open to consider options to increase shareholder value and stakeholder value. And the Board and management are also fully aware of their fiduciary responsibilities when such discussions might happen.

And so it's a constant process at Qiagen where we are constantly looking at the best way to improve value for our shareholders. So I think this is why I continue to say that those processes are natural, long-lasting processes. And the transition with the new CEO should not be viewed as an obstacle to constant improvement of shareholders' value, obviously not. So the 2 processes are going together.

Your next question comes from the line of Tycho Peterson with Jefferies.

I want to start with QuantiFERON. You came ahead this quarter, but then you did soften the language on the full year target to "working towards $500 million." Are you baking in incremental headwinds from competition here in the back half of the year? I guess what's changing in the guide on QuantiFERON? And then a follow-up -- just a follow-up on Jack's question.

On the strategic review, what's really on the table here? Is this portfolio changes? Is it restructuring? Is it a different mix of capital allocation? I mean you've done a lot. You've gotten rid of NeuMoDx, you're paying a dividend. You have good margins. So I'm just curious how you think about the option set as you do the strategic review.

Let me start with the second part of your question, Tycho, and then I will move to QuantiFERON. We are having constant broad strategic reviews. First of all, as you know, we have always said that this company should focus, and we focus where we can gain the most market shares and when we can establish leadership position. This is why we are constantly reviewing the profitability and the return on investment of our different developments in R&D. So it does include the constant assessment, obviously, of our different pillars of growth.

Second, it involves also, as I said before, to be always open for discussion as long as we see that it can create value on the long term for our shareholders, for our stakeholders and also when we see a feasibility to a potential basically alliance for another -- with another company. So it's basically a very thorough analysis on everywhere we can make progresses to create more shareholder value. On QuantiFERON itself, I believe we took the right decision at the end of Q1 when we saw the real decrease of migrant testing to take out $35 million of revenues. We said at the end of Q1 that we don't believe that this situation will change drastically in the coming months, the second half of 2026 or even beyond that. That was the right decision to be taken.

At the same time, Tycho, we continue to very much make progress in other applications and the development of market shares. First, we continue to convert TST customers to blood test with our latent TB testing. Second, we continue to enter into new applications. We told you 2 years ago, for example, that diabetes was becoming an interesting testing field for latent TB. And if you remember, we said in 2025 that we believe that patients ongoing dialysis were also a significant application potential for latent TB testing. We are starting to implement that.

For example, with significant testing labs in the U.S. with the group DaVita, for example. As regard to competition, the fact that new competitors are coming to the market is showing that Qiagen was right many years ago to decide to invest into latent TB testing because I remind you, there is a significant need worldwide for this kind of testing. We showed clearly in our IR session last year that 2 billion people in the world are impacted by latent TB. So the fact that new competitors are entering the market can be seen also positively because it will increase or continue to increase awareness for this kind of testing.

And therefore, for me, it's probably going to increase the total available market for latent TB testing worldwide. For H2, now more precisely to your questions. The first thing, first of all, to highlight is, as we highlighted with Roland, Q2 returns to positive growth. We also highlighted in our press release that in Q3, we are going to be slightly impacted by a very strong comp of Q3 2025, especially in the U.S. But overall, we believe that H2 will return to growth, and then we can achieve our target to keep $500 million revenues for QuantiFERON overall. Growth will strengthen as we move into 2027 with our 2 new major development, the partnership with Inpeco and the AI scored results that we are going to launch towards the end of the year next year.

Competition has always existed Tycho. Our main competitor is the traditional skin test. We had an existing competition for many years with Revvity, and we have seen the market new entrants. At the moment, we do not see an impact on our market shares. We are prepared to compete commercially and product-wise against any new entrants. But I repeat, the main competitor remain the TST and our main objective remains to continue to convert more TST customers to blood testing.

Your next question comes from the line of Michael Ryskin with Bank of America.

First, I want to ask real quick on capital deployment. You had a share authorization at the AGM, but yet it doesn't look like you bought back any shares in the second quarter. Just curious why. Is this have something to do with the strategic review where you kind of want to get that finalized before you deploy capital? Or is there some reason you kind of held back? And I'll throw in a second one, if I can, at the same time.

On the Sample Tech business, that continues to do really well, both organic and Parse. You kind of talked about some of the upside to Parse. And obviously, you've got a lot of the automation coming in the new products that you've talked about. Just want to maybe get a sense of your thoughts on that, how that plays out in the second half as you got a little bit tougher comps and beyond, both on the organic and new launches and also on what the upside from Parse could be.

So thanks, Michael. And I will take the first part, and I will ask Roland to chime in on the capital deployment strategy. As you noticed, you're right, Michael, it's going very well, but it's a proof that our automation strategy that we started back in 2021 is paying off. I remind you, we started to upgrade some of our existing instruments. QIAcube became QIAcube Connect, EZ1 became EZ2. And this year, we have those 3 new launches.

So organically, this is the proof that this strategy is paying off. We continue to see good growth in automated sample tech, and we are absolutely convinced that more customers will move from manual sample tech to automation. So we are having the good set of answers. This is strengthened by the acquisition of Parse because it allows our sample tech portfolio to move into single cells, and we invested and acquired Parse for 2 main reasons. First of all, because the solution of Parse is very highly differentiated compared to existing competition.

First, as you know, it's an instrument-free solution. So the ease of use is uncomparable. But at the same time, to address the large volume needs, we can offer also solution with what we call our GigaLab with Parse. And we see that activity also growing very well. The second main differentiation is the number of sales that we can cover with the Parse solutions, which is also uncomparable. This is, for example, behind the fact that we have been chosen by NASA as we highlighted during this call. We told you last year and at the beginning of this year, that the contribution of Parse into our revenues for '26 should be around $40 million.

With the development of Q1 and Q2, we believe that we have this number into control, and we can probably exceed it. And now going to Roland for the capital allocation strategy for the coming months.

Mike, there's always a lot of reasons when to do and when not to do a share buyback at the end of the day. But one thing you have to have in mind, after an AGM, typically debt holders have an opposition period and that in Europe takes somewhere between 2 and 3 months. It's more technical. Typically, there's never any feedback, but you have to wait for that.

Your next question will come from the line of Odysseas Manesiotis with BNP Paribas.

I've got 2. Firstly, on the organic growth acceleration implied by your Q3 guide, specifically, I mean, on the midpoint organically, I'm getting around 50 bps acceleration. Wouldn't it be fair to assume improving growth in Sample tech, QIAstat and PCR and nucleic acids given your instrument launches, easing comps and improving funding releases here. Could you help us piece out the divisional growth here relative to Q2 and Q3?

And secondly, could you -- I mean, looking at QIAstat, Q2 growth underperformed most of your peers here. And I understand you're relatively more reliant on respiratory, given you're still early on with the GI launches and meningitis, but you held up relatively better in Q4 and Q1. Could you give us some additional color on the Q2 weakness, please? And have you started seeing more U.S. wins since the Rise launch?

So different questions. I will start with QIAstat and then move to Q3 and versus Q4. QIAstat, I wouldn't say Odysseas, that we are more exposed to respiratory panels than our competitors. Respiratory panels in syndromic testing account for roughly 65% of the total volume of testing. So it is clear that everybody is sensitive to a stronger flu season or a weaker flu season. Q2 is never -- if you look at our trends in testing for QIAstat over the last years, a very strong quarter for respiratory. Why? Because you are coming out of winter, but in the Northern Hemisphere. And at the same time, you are not completely in winter in many other parts of the world.

So this explains the weaker numbers on respiratory. It is true that for the last 12 months, us, but also our competitors are seeing weaker flu season. At the same time, and this is the objective of our strategic vision of developing the menu of QIAstat, we are extremely pleased by the very good growth of GI. The relevance also, you have seen the cyclospora example that I gave today. We have meningitis developing very well, especially in Northern Europe, but also starting in the U.S. And we will have for the second half of the year, the BCID panel because as we said today, blood infections are key issues for customers. We now have that blood culture panel CE marked. We expect to have it FDA approved during the fourth quarter of this year. This will help the growth. A second good factor that will help the growth in end of Q3 and Q4 is that there will be a winter again in the Northern Hemisphere.

The problem is not that much to know whether it's going to be a strong flu or weak flu. There will be flu. And here, we will be relevant. And here, you will see an acceleration of our respiratory testing. In the U.S., which remains the main market for syndromic testing, as you know, we have taken significant decisions from an organization standpoint, new sales, salespeople on the field, more specialized, new leadership. This is starting to pay off. And indeed, to your point, where we have the largest volumes of customers, we start to see a good uptake of our QIAstat Rise instrument in North America. So that's the context for QIAstat. And this is why we are confident in a double-digit growth for the second half of the year for QIAstat.

Now coming back to your point on Q3 versus Q4. I mean in Q3, we will continue. We have no reason to consider that, for example, Sample tech will slow down. We believe that Sample Tech will continue to perform well because, again, in Q3, we will be more uptake -- we will see more uptake of our new launches, and we see the continuous development of parse. Digital PCR will continue to perform well. Overall between Q3 and Q4, you will see a continuing good development of capital sales and consumables, and this will be also strengthened by the launch of our new set of panels around gene expression.

At the same time, as we disclosed today, we know that Q3 will be impacted by a very strong comp on QuantiFERON, especially on North America from Q3 of 2025. This is how we see the development of Q3 versus Q4. Obviously, if we can beat our target for Q3, we will do it. But it's, I think, a very mature and realistic analysis to set that guidance for Q3 and also that acceleration for Q4.

And just one incremental comment to that because I do think while everybody has it somewhere, I just want to put it also play on the table, right? We shouldn't forget that, again, there's $35 million of immigration sales for QuantiFERON, which are as a market, not accessible for us anymore for anybody. And if you just put that in the percentage growth rate, that is more or less already 6% to 7% growth rate. So again, at the end of the day, that is what we have to compensate. And again, last year, as Thierry just mentioned, Q3 was an 11% growth rate for QuantiFERON. So it is a very strong comparable quarter.

The rest of the business is actually, as I said, hard to complain sample prep double-digit second half, QIAstat double-digit second half, QIAcuity double digit. Again, I don't think that we can complain too much. And also again, the headwind Q1 next year on QuantiFERON is history.

Your next question will come from the line of Dan Arias with Stifel.

Thierry, on the fully automated QuantiFERON solution that you're bringing to market. I know none of this product development is easy, so I don't mean to trivialize the effort. But why 1.5 years to get that product to market? What are the major steps or hurdles to getting that to customers maybe ahead of another competitive option getting into the market?

Well, because first of all, you need to develop 2 new instruments and adjust them to the specific workflow of QuantiFERON. Those 2 new systems are a dedicated aliquoter and a dedicated incubator. And then you have to make sure that you can connect all those pieces together to build that first fully automation sample in, result out. So to your question, developing and adapting 2 new instruments in, I would say, something like a year, it's quite a performance -- it's quite a performance.

And then obviously, we need to test it with customers. It will be an investment on their side, and we will need to make sure that it is perfectly adapted to their workflow. So there will be some customization. We will work, and we have started to work, especially with our key accounts on making sure that, that workflow from a footprint, from a volume is going to be completely adjusted to their needs. What makes me very confident is that we have started introducing this workflow with a fairly deep level of details to our main customers, main key accounts in the U.S., main key accounts in Europe.

And the acceptance, the interest, the welcoming of this presentation is even beyond our expectation with many sites indeed asking to be the pilot site for this fully integrated workflow. But you still need to develop those instruments. You still need to make sure that the workflow is seamless. And I believe that a year to 1.5 years is not that long. You need to validate also the workflow. You need to push it to regulatory approval.

So second half of '27 is a realistic time line, and I continue to believe that there will be first installation in that time frame.

Next question will come from the line of Dan Brennan with TD Cowen.

Maybe I'll just ask 2 and then kind of mute and listen. Maybe on the first one, Thierry, I think you mentioned upfront to, I think, Jack's question on the strategic plan, both internal efficiency gains and also looking at potential strategic acquirers to maximize value. Could you just comment how management and/or the Board think about private equity versus strategic acquirers?

Are they the same? Are they different given PE will typically look at deals and be more cost cut driven versus strategic corporates are going to be probably more growth interested? And then, I guess, b, maybe as we look ahead and kind of when we turn the page, I think consensus right now sits at 5% CER for 2027. So a decent rebound in easy comps. Just wondering if you guys can offer any initial thoughts about how you're looking to exit this year and kind of what that sets up for next year?

Well, I would say on the first one, first, I will highlight something because I heard twice in that call the end of the process. And this is not the message that I want to leave with you guys. There is not a date end of a process of continuously assessing the best pathways forward for Qiagen. It's a continuous project. Very regularly during the year, management is reviewing and assessing those options with our Board. And we are not going to stop that at a given point.

I think it's management's responsibility to constantly present to the Board options for better shareholder value. So that's the first thing. Now on your question, [ P ] versus strategic, first of all, as you know, Dan, I won't comment in too many details. There are pros and cons on both sides. This is not what is our main driver. Our main driver is to decide, is it better for Qiagen with our midterm plan, with our objective of sales, profitability, return to shareholders? Is it better to continue organically and independently? Would that make sense to have a strategic partner? Or would that make sense to have a more financial-driven partner? What of those solutions is driving the main shareholder value?

For our shareholders, but also for our stakeholders, the Qiageners, the legacy that we have built for more than 40 years now. Now regarding the consensus, and Roland, feel free to chime in on this. We are not in a midterm call here, Dan. So I will clearly say our ambition as management for the moment is to deliver on Q3, is to deliver on Q4 to deliver the full guidance that we gave at the beginning of this year. and to continue to improve profitability. The market has not become easier around us. And despite this, this company continues to deliver profitable growth. You have seen that in Q2. That's my main target. We have a target set since our Capital Market Day in June 2024. We are still working towards that. That's what I can say at this moment.

The last question comes from the line of Jan Koch with Deutsche Bank.

My first one is on instruments. You reported a low teens decline in Q2 despite mid-singledigit growth in Sample Tech instruments. in which product category specifically have you seen the highest declines? And most life science companies have actually highlighted improving order trends in lab instruments in Q2. So are you seeing similar trends? And secondly, on QIAstat, how is the development of the complicated UTI panel progressing? And yes, when could you launch this test? Based on the high clinical need for this solution, how do you see the financial opportunity?

So let's start with stat and the CAUTI, and then I'll go to the instrument trends and capital sales. The reason why we have extremely good expectation on these complicated UTI panels are mainly twofold. First of all, because, Jan, as you highlighted yourself, this is a significant unmet need for clinicians and for labs all over the world. And once again, you need to understand, we are not talking traditional UTI. This is covered by mainly chip solutions. We are talking about complicated UTI, life-threatening UTI.

And there, this is where we have a significant unmet need. And this is a good segue to the second reason to be optimistic is that none of our competitors will have this panel. And to date, none of our competitors have announced that they are developing such a panel. The development progresses very well, and we are still confident that this test will be available for Europe, Europe first in the second half of 2027.

And when I say that, I mean, obviously CE Mark, and then we will move to the U.S. You need to understand, Jan, that any time you launch such an innovative panel, there is a period of time where you will have to do clinical and medical education. I have no doubt that our prospect will immediately see the value of the panel, but you need basically to help them changing their testing habit. It always takes time. So we will have to invest in medical education. But the potential of that test, given the unmet need that I highlighted at the beginning is significant.

And this will be a very good tool, as we said before, to also help mitigating the respiratory panel going high or going low, depending on the strength of the respiratory season. So it's a very good development. It's a very good strategic development. Now on capital sales. We have said and we continue to say and we have said this even starting in '25, we do see indeed a sequential improvement of funding for research and academia. And this obviously helps capital sales.

At the same time, we also highlight that despite that sequential improvement in Q2, for example, compared to Q1 of '26, the NIH outlay year-to-date '26 is still lower than '25. So we remain cautious. We see good progresses, but we remain cautious. And as Roland highlighted in his comments, when you launch a new instrument such as QIAsymphony Connect, such as QIAsprint, for example, Jan, you need to spend some time with customers to validate the new instrument to adjust it to their own needs. That takes a bit of time.

So this is why we see that performance of Q2 for capital sales at Qiagen, still lower funding and at the same time, progressive uptake of our new launches. This is how you should see that. But those are good investments for the future. You will see a significant level of QIAsprint placement when we will disclose the numbers at the end of '26. This is creating growth for the future. You will see good placement of QIAsymphony Connect. This will create consumables for the coming years.

And as Roland highlighted as well, we will launch also the QIAmini. So if you combine those 2 factors, new systems plus sequential improvement of funding, this gives us good reasons to be optimistic.

This is now -- there will be no more -- this is the end of the Q&A session. I will now turn it back to Daniel for any closing remarks.

Thank you. I would like to close this conference call, and thank you for your participation. If you have any questions or comments, please do not hesitate to contact us. Thank you very much.

Ladies and gentlemen, this concludes the conference call. Thank you for joining, and have a pleasant day. Goodbye.

Ladies and gentlemen, let me welcome you to this annual general meeting of QIAGEN. My name is Stephen Rusckowski, I serve as the Chairman of the Supervisory Board. I'm joined today by my colleagues from the Supervisory Board, Bert van Meurs, Eva van Pelt, Eva Pisa, Mark Stevenson and Elizabeth Tallett. We're also joined by 2 Managing Board members, Thierry Bernard and Roland Sackers. We're also joined today by Casper Nagtegaal to my right. He's a partner for De Brauw Blackstone Westbroek, and Mr. [indiscernible] from our auditors, E&Y.

Before we begin the agenda, let me take a moment to go through a few procedural details. First, this meeting is being webcast live on the Internet, and the audience is in listen-only mode. Second, in accordance with past practice, all shareholders present or represented at the beginning of this meeting will be deemed to be here for the entire meeting. The official language shall be English. Mr. Nagtegaal will formally -- has been formally appointed as the Secretary. If we have any questions in Dutch, he will translate them along with our answers. The record date for shareholders and entitled to vote by proxy was May 27, 2026. On that date, the total number of shares with voting rights accounted to 206,250,011. Mr. Nagtegaal, would you please hand me the attendance list, let me count the votes present and represented at this meeting. Thank you.

According to the attendance list, I can inform you that the holders of 165,431,591 common shares in the capital of QIAGEN are present or represented at this meeting and may cast the same number of votes. This represents more than 50% of the issued share capital.

So with that, let us move on to agenda item two. This involves the Managing Board report for 2025. I'd like to first invite Thierry to discuss our progress in 2025. And then we'll have Roland give us a financial update. Thierry?

Thank you, Steve, and welcome, everybody. Thanks for being with us today. First of all, I'd like to begin by thanking our Board for their constant support for the challenges during those years. And when I say Board, I thank not only our long timers, or should I say old timers, but also our newcomers to this Board.

Second, obviously, you will hear today the evolution of Metin Colpan as Honorary Chairman of QIAGEN. And I would like to take advantage of this short introduction to pay a tribute to Metin Colpan as Co-Founder of QIAGEN. His contribution and his guidance to our -- especially research and development over the last years has been nothing short of remarkable.

Last and at least, obviously, I'd like to pay tribute to our close to 6,000 QIAGENers all over the world for the work they have been developing over the last year and especially in 2025, which, as you will see, has been another solid year of execution for our company. And obviously, I would like also to thank all of you, our shareholders, for your attention to our development and your support.

I'm not going to go through the details of all the slides because most of you, I assume, are quite familiar with our company. But as a reminder, as you see here, QIAGEN has been developing for the last 40 years, added value, molecular solution -- molecular biology solution for research, for academia, for clinical, for pharma companies. It's a worldwide company of a bit more than $2 billion. As you all know, it's listed in Germany, listed in the U.S. as well, a member of the DAX index in Germany.

And I was -- I would like to highlight on this slide that it's a remarkably balanced company. What I mean by this, first of all, it's typical, what we call razor-razorblade business model, where 90% of our revenues are quite recurring. We are talking about consumables, kits test for biology, and 10% made of instruments and services.

Second, you see also a remarkable balance between what we are selling to what we call life science customers, basically research and academia, or also clinical customers, clinical hub, lab, hospitals, pharmaceutical companies. It's 50-50 of our business.

And last but not least, I will insist also on the remarkable balance from a geography standpoint. We are not depending on one single geography. It's a worldwide company, obviously, with the tremendous importance of our sales in North America but also Europe and some emerging countries.

There is something unique about this mid-cap, is that I can guarantee you, it is not the first time and the first year that I'm saying that, that no researcher, no PhD in the world doesn't know QIAGEN, and for one reason is that 40 years ago, this company literally revolutionized and standardized what we call the first step of any molecular biology run, which is the sample preparation.

And this massive leadership in sample prep gives us a unique position. Instead of going through that slide, let me give you 3 examples of how relevant this company is. You probably remember from last year that picture that was all over the world of policeman at the entrance of the Louvre Museum in France because of the robbery that happened there. At the feet of those policemen, you had 2 boxes, it was QIAGEN. It was QIAGEN product.

You might have seen for those of you being on Netflix, one of the recent blockbuster in Netflix called The Pitt. Guess what, in The Pitt, once at the point, there is a nurse in the hospital suspected of an infection potentially from a patient of tuberculosis. And what the doctor said? You need to use QuantiFERON, a product by QIAGEN. Or last but not least, there was a documentary on Ed Sheeran, the singer in Europe. Guess what, they did a DNA analysis of one of his hair. Who did they use? QIAGEN as well. That's the relevance of the company.

So let's go very quickly into the successes of 2025. And I'm going to go quite fast. Roland will go into some more details on the financials.

'25 has been another year of solid execution for this company. You remember from previous presentation that we focus into what we call 5 pillars of growth. And you can see here in that slide that in '25, we once again executed perfectly on our guidance. So execution on sales, 8% growth of those 5 categories of product, it's above market growth, perfectly in line what -- with what we said to the market. It's also an achievement, execution on research and development. Not only did we deliver on sales -- but all of our research and development product. And you remember that QIAGEN allocates roughly 9% of our sales to research and development are perfectly online or on target or did hit the market.

We started to launch new instruments in sample tech. We have a new chemistry, for example, for latent tuberculosis. We started to launch new assays on digital PCR, new assets also on syndromic testing. So execution on sales, execution on development. And this obviously is planned to continue in 2026, where we want to continue to invest into those 5 priorities. As a couple of examples. This company is currently launching 3 new instruments on the market on sample preparation.

This is unprecedented, launching new partnership in full automation for tuberculosis. New assays for gene expression in digital PCRs, new assays on syndromic testing

And for example, this NVIDIA agreement for our bioinformatic activities. I know I go fast, but I will be open to questions on -- if you have any, at the end of this presentation.

Execution on sales, execution on research and development, execution also on capital allocation. You probably remember that for the first time last year, we introduced dividends for our shareholders. We also executed again on return to shareholders via share buyback, the last one being in Q1 of 2026 for $500 million, but we also executed on smart bolt-on M&A, acquisition of companies that are very synergistic with our current product portfolio. And I would highlight 2 examples for '25, the acquisition of Parse Biosciences, a company in the U.S. specializing in single cell, a natural extension of our activities in sample prep. And the company, Franklin, adding new capabilities to our bioinformatics, a company headquartered in Tel Aviv in Israel.

Because I'm sure you follow our company, you saw that Q1 of 2026 was a bit of a more difficult quarter. For the first time, in 27th quarter, we missed guidance. But we missed guidance on the top line, on sales only. We maintain and we achieved guidance on profitability. What I would highlight, it's a mixed bag of results because of one element. We were taken, to a certain extent, by surprise, by the complete slowdown of immigration testing for tuberculosis, especially in the U.S., and that impacted our numbers.

The rest of the portfolio delivered quite well on target compared to our guidance, but this bad result on QuantiFERON pushed the company to update its guidance for the year, not only on sales, lowering it to between 1% to 2% of sales and adjusting also our target for EPS at $2.43. This is mostly driven by a difficult environment on our market.

Capital, money, research money is not flowing as fast as we expected. This is mostly the case in the U.S. And as we said, some hiccups like lack of migrant testing for tuberculosis. At the same time, for the last 5 years, this company has been forcefully focusing not only on growth but on profitable growth. You remember that we presented last year the program, multi-annual program that we call QIAefficiency, where we committed to the market to deliver since 2024, more than 250 basis points of additional operational efficiency. And we are doing that with different actions.

We completely changed the organization. We try to delayer QIAGEN process optimization with our upgrade of a new ERP system with SAP HANA 4. We have streamlined our portfolio when we consider that some activities were not profitable enough, and we did not hesitate to divest from them, and we constantly try to optimize our network of sites all over the world.

Last but not least, obviously, and this is not something new for our company. We are investing for more than 10 years now in AI capabilities, not only to streamline operational efficiency, but also to help for product development. All this in a context where we continue to heavily invest into ESG activities either through people, look at the numbers around, for example, diversity, environmental responsibility, our net zero commitment to the market that we took 3 years ago, but also from a regulatory and governance standpoint.

As a nutshell, in closing, 2025 was another very solid year of execution for QIAGEN. It's fair to say that we have the Board, we have the QIAGENers, the people. We have the solutions and products, and I think we have the shareholders to continue to be successful.

Thank you very much, and passing to Roland now for more details on the P&L. Thank you.

Thank you, Thierry. Before I invite Roland to come up to the podium, I'd like to say that what we'd like to do after we have the presentation of Roland, is at that time, we'll take all your questions for all the agenda items at our meeting. We find this approach best serves you and providing an opportunity to discuss a wide range of topics. Then I will briefly introduce the agenda items, which we're required to do, and we'll take a vote to each of them.

So with that, Roland, it's yours.

Yes. Thank you, Steve, and thank you to everyone joining us here in person. It is good to see you again.

Before I begin, I want to take a moment to recognize Dr. Metin Colpan. As a Co-Founder, our first CEO, and a member of Supervisory Board for more than 2 decades, Metin shaped QIAGEN from the very beginning. Let me express my personal appreciation for his extraordinary contribution over more than 4 decades. And thank you for your dedication, your leadership and your commitment to QIAGEN.

Before I start, let me point out our disclaimer. Today, we will be making forward-looking statements and providing you with responses to questions that involve our intentions, beliefs and views about the future. You can find further information on our website at www.qiagen.com.

So let me now review our results for 2025, a year in which we delivered on our commitments. We reached the high end of our sales outlook and exceeded the adjusted earnings outlook. Sales grew 5% at constant exchange rates, or CER, and this was a solid performance in challenging market conditions, while sales on a reported basis rose 6%.

We again delivered improved profitability as the adjusted operating income margin rose to 29.5% of sales from 28.7% in '24, an increase of about 0.8 percentage points. And we exceeded our target for adjusted earnings per share while also increasing our target twice during 2025. Operating cash flow remained at the high end of $654 million even after absorbing cash payments for efficiency initiatives and higher CapEx investments into our IT infrastructure.

We continue to deploy capital in a disciplined manner. At this AGM, we are proposing a 40% increase in our annual dividend to $0.35 per share. We are also seeking shareholder approval for additional share repurchase authorizations. This will provide additional flexibility to return capital to shareholders while continuing to invest organically and consider value-creating M&A opportunities as we have done recently with acquisitions of Parse and Genoox. To summarize, '25 was a solid year that again reinforced the value of our portfolio, the strength of our execution and the power of our financial position to enhance growth and value creation.

Moving to the next slide. I would like to review the key financial figures under U.S. GAAP accounting standards. Our sales were USD 2.09 billion for 2025, rising 6% on a reported basis compared to '24 in a demanding economic environment. Currency movements had a positive effect of 1 percentage point of net sales, while sales up 5% at constant exchange rates compared to our target for 4% to 5% CER growth. For the full year, the adjusted operating income margin was 29.5%, an increase of 0.8 percentage points from 28.7% in '24.

R&D expenses were 9% of sales and in line with our target. Sales and marketing expenses declined to 21.9% of sales from 22.8% in '24 as we maintained a high level of customer engagement with increasing use of digital channels. General and administrative expenses rose slightly to 6% of sales in '25 amid a period of higher IT infrastructure investments. Adjusted earnings per share for '25 under U.S. GAAP accounting standards was $2.38, an increase of 9% over '24, and these results were also above our target.

Moving to the next slide. Let me review our sales among the 4 product groups. Let's start with Sample Technologies, the heart of QIAGEN and contributions about -- and contributing about 1/3 of sales. This rose 2% at constant exchange rates despite cautious customer spending, especially in the U.S. Diagnostic Solutions is our second product group, and here, sales were up 6% CER. QuantiFERON rose 10% CER, supported by ongoing conversion gains in the latent TB testing market that is still only about 40% penetrated. For QIAstat-Dx, our system for syndromic testing sales rose 24% CER as we benefited from the full core menu in the United States and a growing installed basis that exceeded 5,200 instruments at the end of '25.

Moving to the PCR nucleic acid amplification product group. This year, we're up 1% CER compared to '24, led by double-digit consumable sales growth in our QIAcuity digital PCR systems. We surpassed more than 3,200 cumulative placements of QIAcuity since launch. At the same time, we saw lower sales of other PCR consumables, which includes the OEM business, due in part to timing of customer contracts and funding constraints.

Sales in genomics NGS product group were up 2% at constant exchange rates from '24. The QIAGEN Digital Insight bioinformatics business delivered solid growth in '25, supported by demand across both discovery and clinical customers.

Moving on to our margin development in '25. We saw a good increase of 0.8 percentage points in the adjusted operating income margin to 29.5% of sales in '25. Underlying profitability improved significantly since this improvement more than -- since this improvement more than offset about 1.2 percentage points of combined headwinds from tariffs and adverse currency movements. A key contribution factor has been our QIAefficiency program. To give you a few examples, we benefited from portfolio optimization measures, particularly the phaseout of NeuMoDx that was completed in mid-'25 as well as a continued focus on cost discipline around QIAGEN. These initiatives are enabling us to deliver higher profitability while continuing to invest in innovation and enhance future growth opportunities.

On this slide, I would like to show you a reconciliation of the reported U.S. GAAP results with the adjusted results. These adjustments are in line with those of our peer companies and provide transparency for investors comparing QIAGEN with other companies. As you can see, the largest adjustment was related to business integration, acquisition and restructuring-related items. The adjustment to operating income was $150 million, and this reflects the charges related to the acquisition of Genoox in May '25 and Parse in December '25. It also included costs related to the efficiency measures. At the same time, about $63 million of these charges involved noncash items.

As a Dutch company, we are required to report results under IFRS or International Financial Reporting Standards. On this slide, you can see a difference in net income of about $12.1 million between U.S. GAAP and IFRS results. The most significant factor relates to the IFRS accounting for the fair value of the convertible notes. Under IFRS, the conversion features of these instruments are treated as liabilities. Under U.S. GAAP, these are considered in equity. Accordingly, the revaluation of the convertible notes has an impact on the income statement under IFRS. Another difference relates to restructuring costs. Under IFRS, certain personnel-related accruals are recorded later than under U.S. GAAP. In '25, this resulted in higher costs of $4 million under IFRS.

Furthermore, development expenses are handled differently. Under IFRS, internal development costs are capitalized, amortized over a multiple year period through cost of sales. Under U.S. GAAP, they are expensed immediately. Most institutional investors use U.S. GAAP results when comparing QIAGEN with our peers. This is why U.S. GAAP remains the primary basis for presenting our results to the financial community.

Turning to the next slide. We are using our cash flow and financial strength to support the business expansion through organic and inorganic opportunities, while also increasing returns to shareholders. In terms of cash flow for 2025, operating cash flow was USD 654 million and absorbed about $54 million of cash payments for the efficiency initiatives.

At the end of '25, our leverage ratio was 0.7x net debt to adjusted EBITDA compared to 0.3x at the end of '24. This reflects the impact of deploying cash for the dividend, the synthetic share repurchase and targeted acquisitions. We returned approximately $300 million to shareholders through a synthetic share purchase program in the early '25 and also the introduction of a dividend payment in '25.

On this slide, you see our financing structure as of December 31, 2025. In terms of our balance sheet. Total consolidated net debt stood at USD 556 million at the end of '25 compared to $239 million at the end of '24. During '25, we successfully refinancing approximately $500 million of maturing debt through the issuance of a $750 million convertible note. This transaction extended our debt maturity profile, strengthened our financial flexibility and positioned us well to support future growth initiatives and capital allocation priorities.

Our employees remain at the center of QIAGEN's success. At this slide, you see a profile of employees by regions and function. We continue to attract and retain talented employees by providing interesting and rewarding opportunities along with a pay-for-performance culture. At the end of '25, the total number of employees declined to a low 5,700 compared to nearly 5,800 employees at the end of '24. This reduction reflects a decision to discontinue NeuMoDx and DIALUNOX products as well as the impact of targeted efficiency measures. All workforce reductions are handled in a socially responsible manner and in line with local laws. While the overall head count declined, we continue to recruit in strategic growth areas, particularly to support new product development and commercialization.

On the next slide, I would like to update you on our investor relation activities in 2025. We currently have 22 analysts covering QIAGEN and this includes the leading banks of the world. Our teams continued our deep dive series of online broadcast focusing on QuantiFERON and sample technologies in 2025. They provide a noble way for us to engage with the financial community and explain the pillars of our portfolio. In fact, this innovative series was recently recognized in the annual IR impact awards shortlisted among the top 5 nominations, including for the best innovation in shareholder communication. You can watch this broadcast live on our website.

Turning now to the share price performance. While market sentiment towards the life science and diagnostics sectors remained challenging during '25, QIAGEN shares demonstrated relative resilience compared to many of our peers. For '25, our shares in New York declined 2% in U.S. dollar terms. This compares favorably with the broader diagnostic peer group that declined 22%, and our diversified peer group, which was down 4%. In euro terms, our share price in Frankfurt was down 12% compared to the end of '24, primarily reflecting currency movements of the euro strengthening against the U.S. dollar.

Turning to my last slide. I would like to quickly summarize the key messages. First, QIAGEN delivered another year of growth led by our growth pillars despite a challenging market backdrop. Our teams exceeded the outlook we had set for adjusted earnings, while net sales came in at the high end of our outlook. Second, we expanded profitability through efficiency gains and focused execution despite currency and tariff headwinds. Third, we generated substantial free cash flow, providing flexibility for investments and shareholder returns. And finally, our capital allocation strategy continues to prioritize the highest value opportunities, combining investments in growth, with increasing returns to shareholders.

As we look ahead, we remain focused on helping customers achieve better outcomes, improving patient care and creating sustainable value for shareholders. With leadership positions in attractive growth markets, a differentiated portfolio and a great workforce, we are strengthening the foundations for future growth. The combination of our differentiated portfolio, strong profitability trends, healthy cash generation and focused capital allocation positions QIAGEN to create sustainable long-term value for all stakeholders.

Thank you very much. And with that, back to Steve.

Thank you, Roland. We now have an opportunity for your questions on all of the agenda items. Please?

Yes. Good morning to all. My name is Andreas Massek from the SDK, Schutzgemeinschaft der Kapitalanleger, which is a German shareholder association with around about 8,000 members.

Let me come to the agenda and putting some questions. First question. Why was the meeting scheduled for very early 9:00 this morning? You can imagine that this time is very inconvenient for those shareholders from abroad who want to attend in person. It seems more to be a meeting for the Board members than for us shareholders.

I estimate that the remuneration report is part of the financial report. It has been fully audited by the auditor in connection with the annual financial statements. Is that correct?

While the amount of the proposed dividend does not follow the SDK's policy of distributing 40% to 60% of net income to shareholders, it must be seen in the context of other shareholder return generating measures. Share buybacks are also to be carried out with the synthetic version resulting in monetary payments. What criteria were used to calculate the dividend?

Concerning the proposal to repay to the shareholders an amount, which at maximum, will be USD 200 million in the aggregate. What criteria were used to come to the USD 200 million? And also interesting would be what and when -- what, which amount? And when will you pay it for this year?

Point of -- item of authorization of the Managing Board until December 2027 to acquire shares in the company's own share capital. What will be the plan for this in detail? By the way, the SDK prefers the payment of a dividend as a direct shareholder remuneration versus a share buyback.

Please note that for reasons of principle, the SDK rejects the mandate of Ernst & Young companies until a complete clarification of the events at that time and the resulting consequences for [ EY ] has been carried out in the Wirecard case. You may know that this has been a big scandal in the German capital market some years ago.

Regarding Item 16, QIAGEN has been planning continuous share buybacks so far and in the future, so that the usefulness of capital increases is not apparent. What is the background of this proposal?

We heard some rumors about the acquisition of QIAGEN by, for example, Thermo Fisher, Danaher or Agilent. Are there any actual considerations or negotiations running concerning any acquisition of QIAGEN at the moment?

And I would like to ask how many shareholders are, at the moment, online, present, watching or hearing the meeting, if you know that, I don't know. Yes, these were my points.

Okay. Thank you. So let's see, we have a number of questions. Let's make sure we can walk through all of these.

The first question is pretty straightforward, and that is why did we schedule the meeting at 9 a.m. It's my understanding, Thierry and Roland, that it's been our practice of running the AGM at 9 a.m. That's good feedback. We appreciate that. But it has been our practice, starting at 9 o'clock for a number of years, I believe.

We could revisit for next year.

We could revisit that. So I appreciate that.

Second is a -- Roland, question about the remuneration report?

Of course, we have E&Y in the room. So I talk under your supervision, but of course, the remuneration report was fully audited by E&Y as a normal practice. Not, or I guess, you agree. Or sorry, I wasn't -- No. So as I said, E&Y is in the room. So I clearly talk about under your supervision, but I think I see you nodding. So of course, the report was fully audited by E&Y as well. So I think that's a clear yes.

In terms of dividend, while we clearly acknowledge the policy of the SDK, I do think it's fair to say as well and to remind that QIAGEN is clearly seen from many investors and probably also the majority of the investors as growth companies. Nevertheless, we also started with paying out a dividend last year. This year, we announced a substantial increase into our dividend, as I just said before, to about 40% increase. So we'll see how that moves forward.

But clearly, there is, I would say, a tendency to see that QIAGEN is reviewing the allocation of capital every year. And this year, I would say, another positive sign into your direction. We are increasing the dividend gets out, of course, quickly paid out as well. So I would say we are moving into the direction. Nevertheless, we have to clearly understand that we are -- still see ourselves also as a growth company, and that typically, 60% is not what you see as dividend payment.

In terms of -- similar direction on what you asked in general, what we're doing on capital allocation. I would say our general capital allocation policy, while it's involving hasn't changed. That means we are clearly still very strong about this, at the end of the day, 3 different measures.

First and foremost, we do believe organic growth is the most important growth driver for our company. So we're going to continue to invest into R&D and clearly also in other opportunities within the company. If there's any bolt-on inorganic opportunities, we're happy to review that as well if it increase the value for our stakeholders, particularly the shareholders.

And last, but for sure not least, we have a commitment to capital allocation. You know that since 2012, we are doing share buybacks. We started with $100 million incrementals. As the cash flow of the company has evolved very strongly over the last years, we stepped that up. We also used a very Dutch style of synthetic share buybacks, which, as you pointed out correctly, can be -- clearly has also a dividend policy part of in it as well because the capital goes straight to the investors. So I do think that is something that we shouldn't neglect. And therefore, we do believe that, that capital policy covers actually the profile of QIAGEN best.

What we are going to do? This year, again, I can't speak on behalf of the Board, but I do think it's clearly something what we regularly discuss with the Board. We are waiting for the results of today's AGM, assuming for a second that you approve what we recommended to our shareholders, meaning that we have flexibility in share buybacks, but also increase the dividends. I think there is clearly a discussion to happen with the Board when that is, again, dividend will be paid off. Of course, as always, more or less briefly after the AGM, and the share buyback is an ongoing discussion, where we include a lot of different things, from share price performance, all the way down to what we see on the M&A market is going to happen.

Why do we have an authorization to acquire our shares again? It's more or less what I answered here as well. So I think that is into that.

We hear your comment on E&Y. Have in mind, first of all, that we are a Dutch company, and that's one thing. So again, what -- and that's one thing. The second thing, I think it's fair to say, while the AGM is not fully over, I would expect that E&Y gets revoted as last year with more than 99% of all votes casted.

And next question is on any negotiation regarding acquisitions of QIAGEN. I'm not sure, Steve, if you want to take that question.

Sure. Well, it's our long-standing policy. We don't comment on any rumors or speculation about the company, and we continue to evaluate strategic options in the best interest of all shareholders.

And good. Then you had one question, how many shareholders are online? I think we can't see that numbers right now, but I do think what I can tell you, we do expect that more than 80% of votes are casted today on the AGM, and that is probably on the highest what you can see in Germany, but I think also in the European environment. So I do think the participation of our shareholders is very strong in our AGM.

Thank you, Roland. I think [ we have ] of that. So if there are no further questions, let me conclude this portion of the meeting.

So now let us now continue with agenda item three. This is a nonvoting item and concerns the Supervisory Board report on the annual accounts for 2025. You can find this information in our annual report, which is available on our website.

Next, we move to agenda item four. This item involves a nonvoting item and a review of the main items of our corporate governance structure in compliance with the Dutch Corporate Governance Code. As a Dutch listed company, QIAGEN is subject to the Dutch Corporate Governance Code. QIAGEN complies with virtually all of the best practice provisions of code. There are some minor deviations due mainly to legal requirements in our jurisdictions as well as by industry standards. These are outlined in the corporate governance section of the annual report.

Moving to agenda item five or adoption of QIAGEN's annual accounts for 2025. This is a voting item. [indiscernible] from E&Y is here. If here, does anyone have any questions for our auditors? Thank you. We now vote on this item. Is there anybody against the proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record this proposal has been adopted.

Let's move to agenda item six. This involves an advisory vote for the remuneration report, which is based on implementation of policies previously approved by our shareholders. Is there anybody against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby report this proposal has been adopted.

We now proceed to agenda item seven. This is nonvoting and our dividend policy. As you know, QIAGEN introduced an annual dividend at the Annual General Meeting in June of 2025. There is no change to our dividend policy.

Moving to agenda item eight. We will vote on the adoption of the proposal for a dividend of $0.35 per share to be paid out as outlined in the proxy. Is there anybody against the proposal? Is there anybody who would like to abstain for voting?

[Voting]

I hereby record that this proposal has been adopted.

Let us now move to agenda item number nine. This voting item involves the proposal to discharge the members of the Managing Board from liability for performance of their duties during 2025. Is there anybody against this proposal? Is there anybody who would like to -- we recorded it, no? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record this proposal has been adopted.

Now we'd like to move to agenda item 10. This is the voting item involving a proposal to discharge the members of the Supervisory Board from liability for the performance of their duties during 2025. Is there anybody against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record this proposal has been adopted.

Now let's move on to agenda Item 11. This voting item involves a set of proposals to adopt 2 new members and reappoint 6 members of the Supervisory Board for a new 1-year term until the day of the next Annual General Meeting in 2027.

A joint meeting of the Supervisory Board and the Managing Board has unanimously adopted a resolution to have a binding nomination for the following people: Toralf Haag, Robert McMahon, Bert van Meurs, Eva van Pelt, Eva Pisa, Mark Stevenson, Elizabeth Tallett and myself, Stephen Rusckowski. These nominations are made in the context of significant renewal of the Supervisory Board over the past 5 years. Following this meeting, 7 of the 8 Supervisory Board members will have joined since 2021.

The level of review reflects a deliberate effort to refresh and strengthen the Supervisory Board to complement it's already strong profile. This group combines fresh perspectives, deep expertise and proven relevant leadership experience among recently appointed Supervisory Board members with the continuity and institutional knowledge of longer-tenure members to support QIAGEN's future development.

In January 2026, Ross Levine stepped down after taking on a new role at Memorial Sloan Kettering as the Chief Scientific Officer. Let me take this opportunity to thank Ross for his many contributions to QIAGEN, and also express our appreciation that he continues to lead the Scientific Advisory Board. Following this departure in January, Mark Stevenson joined us in that same month. Mark, with over 30 years of experience in life sciences technology companies, in particular, Thermo Fisher, Mark brings operational leadership in global life sciences experience at scale.

We also welcome Robert McMahon as a new nominee. He will join the Supervisory Board after his appointment at this meeting. Bob brings deep expertise from his roles at a number of top health care companies, including J&J, Hologic, Agilent and now West Pharma. Mark and Bob, thank you again for joining QIAGEN.

I'd also like to recognize a person of exceptional importance to QIAGEN, Dr. Metin Colpan. Metin will conclude his service on the Supervisory Board and has decided not to stand for reelection. As a co-founder of QIAGEN and our first Chief Executive Officer, Metin was instrumental in building this company from the ground up. He helped define QIAGEN scientific foundation and brought the entrepreneurial drive, scientific vision and leadership that shaped our early development and long-term direction.

Since 2004, Metin has continued to contribute to QIAGEN as a member of the Supervisory Board. So on the behalf of my colleagues, I'd like to express our deep appreciation for his extraordinary contributions to QIAGEN over many years. Naming Metin Honorary Chairman of the Supervisory Board is a fitting recognition for his lasting impact. As this agenda item also relates to my own reappointment, I'll ask my colleague, Eva Pisa, to take care of that specific proposal.

Now let us move on to voting. First of all, with respect to Toralf Haag, is there anybody against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record this proposal has been adopted.

With respect to Robert McMahon, is there anyone against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record this proposal has been adopted.

With respect to Bert van Meurs, is there anybody against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record this proposal has been adopted.

With respect to Eva van Pelt, is there anyone against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record that this proposal has been adopted.

With respect to Eva Pisa, is there anybody against this proposal? Is there anybody who'd like to abstain from voting?

[Voting]

I hereby record this proposal has been adopted.

With respect to Mark Stevenson, is there anyone against this proposal? Is there anyone would like to abstain from voting?

[Voting]

I hereby record that this proposal has been adopted.

And with respect to Elizabeth Tallett, is there anyone against this proposal? If there is anyone who would like to abstain from voting?

[Voting]

I hereby record that this proposal has been adopted. So I'd like to congratulate my colleagues on their appointments and reappointments.

So now I'd like to ask Eva Pisa to take care of the voting on my own reappointment. Eva?

Thank you, Steve. With respect to the proposed reappointment of Stephen Rusckowski, is there anybody against the proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record that this proposal has been adopted. Before I hand over, I would like to congratulate Steve on his reappointment as Supervisory Board member.

Thank you, Eva. On the behalf of the entire Supervisory Board, I'd like to thank you and our shareholders for your trust and your confidence of me leading the Board.

Now let's move on to agenda item #12. This voting item involves the reappointment of our 2 managing directors. The reappointment would be for a period of the day following the meeting until including the day of the Annual General Meeting in 2027, noting that Thierry will step down after the appointment of a new CEO.

We now move to the voting with respect to Thierry Bernard. Is there anyone against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record that the proposal has been adopted.

With respect to Roland Sackers. Is there anyone against this proposal? Is there anybody who like to abstain from voting?

[Voting]

I hereby record that the proposal has been adopted. I'd like to congratulate both of you on your reappointment as members of the Managing Board.

Moving on to the next agenda item, item #13. This is the voting item on the updated remuneration policy for the Managing Board. A copy of the policy is available on our website. Is there anybody against this proposal? Is there anybody who'd like to abstain from voting?

[Voting]

I hereby record that this proposal has been adopted.

Let's move on to agenda item 14. This voting item involves the reappointment of E&Y accountants BV as our auditors for 2026. Is there anyone against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record that the proposal has been adopted.

Agenda item #15. It accounts to the proposal to appoint E&Y accountants BV as our assurance provider for 2026. This proposal is due to a new European directive that requires an auditor to review our sustainability reporting. Is there anybody against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record that the proposal has been adopted.

Agenda item 16 consists of 2 points concerning the proposal to renew the current designations of the Supervisory Board to issue shares and to restrict or exclude preemptive rights. The first item is agenda item 16A. This voting item involves the authorization of the Supervisory Board until December 24, '27, to issue ordinary shares and finance preference shares and grant rights to subscribe for such shares. Is there anybody against this proposal? Is there anyone who would like to abstain from voting?

[Voting]

I hereby record that the proposal has been adopted.

The second is agenda item 16B. This voting item involves the authorization of the Supervisory Board until December 24, 2027, to restrict and exclude the preemptive rights to issue ordinary shares or grant subscription rights. Is there anyone against this proposal? Is there anybody who like to abstain from voting?

[Voting]

I hereby record that the proposal has been adopted.

Let us now move on to agenda item 17. This voting item concerns a vote on the proposal to renew the Management Board's current authorization to acquire QIAGEN shares. Is there anyone against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record the proposal, and has been adopted.

Now we move to agenda item 18. This voting item involves proposals to authorize the implementation of a synthetic share repurchase through the same procedure used in recent years. Is there anybody against this proposal? Is there anyone who like to abstain from voting?

[Voting]

I hereby record the proposal, and it has been adopted.

Now we are the final item, which is agenda item 19. This voting item provides us with the ability to cancel whole and/or fractional shares. Is there anybody against this proposal? Is there anybody who would like to abstain from voting?

[Voting]

I hereby record that the proposal has been adopted.

So we have completed all of the agenda items. Before I close this meeting, on the behalf of the entire Supervisory Board, we'd like to thank all of our employees worldwide for the contributions to the success of QIAGEN. My colleagues and I have great confidence in our future growth prospects and the impact QIAGEN could have on achieving our vision of making improvements in life possible.

Let me thank each of you for your attendance at this meeting. We truly appreciate your support in QIAGEN, and look forward to our ongoing engagement. Thank you, and see you next year.

Hello, and welcome to our next deep dive. Today, it's all about QIAcuity digital PCR. We're going to answer questions around what is digital PCR, how does it compare with quantitative PCR and how does sequencing fit in. But before we begin, a quick legal note, as with any investor event, this presentation includes a safe harbor statement. You're likely familiar with this from our other presentations, so I won't read it in full. However, please remember that we will be making forward-looking statements. Actual results may differ materially from those projected, and the factors driving those are detailed in our most recent Form 20-F filed with the Securities and Exchange Commission. A copy is also available on our web page.

Let's now have a closer look into how DPCR, qPCR and NGS differ and why it matters. Huw Ricketts our Head of Global Digital PCR and Francesca Di Pasquale, our Head of Digital PCR R&D are going to take us on this journey.

Huw what are we doing here by the lake? I thought we're going to talk about digital PCR.

I know we are, but I thought this would be a great location to talk about it. Earlier, I collected this water sample from the lake here, but don't worry, German waterways are generally pretty clean but this water sample could still contain traces of wastewater.

Now I see where you're going. So let's assume we want to analyze this sample for traces of Norovirus for early signs of an outbreak similar to how wastewater was analyzed during the COVID pandemic.

Right. Good point. It was using the COVID pandemic. So this is a kind of sample where digital PCR can be really valuable. It's a complex sample. In this sample, there contains millions of different components, could be bacterial DNA could be viruses, could be human DNA, could be environmental material.

So how do we find a very small amount of genetic material from virus particles in all of that. There's different ways to approach it, right?

Exactly. And option #1, next-generation sequencing. -- don't look for 1 specific target like norovirus. We look for the unknown, we sequence or analyze all the genetic material in here. And at the end, we have a comprehensive overview of exactly what's in the sample and in what quantities like norovirus, bacteria, human DNA and more.

And with that, at the end, we have a very broad overview of what's in the sample.

Yes.

I know what I'm looking for, I could simply go with, for example, QPCR.

Yes. With QPCR, we don't analyze everything. We look for one known sequence.

And how does that work?

We specifically look for norovirus. We make many copies of it, and then we detect the signal and monitor that over time as it increases. The stronger the signal, the more norovirus is in that but we rely on a reference standard. We compare our sample to a sample where we know how much of the target is in there. We use that comparison to make a calculation of how much norovirus is in the sample.

And what about doing that in a complex something like that?

That's when it becomes more challenging substances in the sample can interfere with the reaction. And if our target is low concentration, it's difficult to detect the signal accurately and precisely.

And this is where digital PCR comes in, right?

Yes. Instead of looking at the whole sample at once, you divide the sample into thousands of different reaction chambers the so-called partitions.

So even with a very complex sample like this and at very low concentrations, we're able to get clear results.

Yes. And this is particularly important in surveillance, where we want to detect very low levels of target over time. For example, during the COVID pandemic, when we were looking at small changes in virus in the community, we want to be able to detect those signals early and with high confidence.

So how does this work in practice?

Detection, quantification and confidence.

Okay. Great. Let's go to the lab.

Let's do it.

So Huw and I, we just took a walk and we used this water sample to explore the difference between next-generation sequencing QPCR and DPCR. And now we need your help to go one step further and have a closer look into QIAcuity digital PCR and how it works in practice.

Sure. What is really interesting is that what you have been exploring now does not only apply to wastewater.

In both environmental and clinical samples, we are really interested in finding a tiny amount of signal within a very large background.

In wastewater, it could be a trace of a virus. In blood, indeed, we could be interested in finding cancer cells or very few amounts of cancer DNA within a large background. Both applications are very different, but the principle remains indeed the same. In this latitude, we have millions of healthy cells. And the key question is, do we also have cancer cells in it? And if so, how many?

And where would we start to find that out?

The first step is always sample preparation. We extract the DNA from the sample. We load the DNA together with the required reagents onto the plate and we seal it. then the plate is put into the QIAcuity instrument and the [indiscernible].

And what happens in inside the QIAcuity?

The sample is partitioned into thousands of single reaction chambers, the so-called partitions. In every petition, a PCR takes place, targeting the cancer markers that we are interested in.

That's right. Each individual partition gives a clear answer.

This is also the reason why it is called digital PCR. Every single partition gives a yes and no answer like the 1 and the 0 in a computer logic. By counting these, the software use statistics to calculate how many cancer cells were present in the original blood sample.

And how long does it take?

The whole process takes about 2 hours. Everything happens in only 1 instrument fully automated and plate-based. And actually, you can also detect more than 1 target at once, up to 12 in parallel, and this is multiplexing. No reference standards, no complex setup, simple, scalable and highly reproducible.

We've seen how digital PCR works and why it delivers precise and reliable results. In real-world applications, it's not about measuring once -- it's about generating consistent results across labs, across studies and over time. But what does it mean for our customers? And why are more and more switching from QPCR to DPCR, let's take a closer look.

Now let's talk about our customers and their applications. So Huw why do customers switch from QPCR to DPCR?

It's all about confidence in your data. Customers are facing increasingly complex samples and demanding applications. They need to be confident they're producing reproducible data across different labs, across different operators and at different times.

So our customers get more out of their samples. They generate higher confidence data and all that at a very similar price point per experiment.

But what makes the QIAcuity really stand out?

It starts with simplicity. The QIAcuity is a fully integrated all in one system that reduces hands-on time and reduces complexity.

And it is also why it is one of the most user-friendly digital PCR instrument available. It really enables our customers to implement it easily and also scale it across different labs and it also fits seamlessly into the QIAGEN ecosystem starting from the sample technologies.

And beyond simplicity and integration?

Flexibility and scalability. Whether you're running a few samples of thousands. We have a 1 plate system for low throughput users to a multi-plate system for the high throughput environment. And that's with all the same technology.

What else?

Speed at scale, QIAcuity is very accurate and highly reproducible across all different throughput levels. A good example is in biopharma, where you may have an R&D facility running many samples, screening many samples, and then in the same system can be used in the manufacturing where quality control measurements need to be made at much lower throughput.

One system, different needs, right?

That's right. One system across all those different applications. All in all, QIAcuity combines performance with simplicity, ease of use, flexibility and scalability.

What about QIAcuity digital PCR in clinical and diagnostics.

Well, we have already shown that digital PCR brings a lot of value in research, but we do not stop there. With QIAcuity-DX, we bring digital PCR to the clinical and diagnostic space.

It forms a strong alternative where sequencing can be too slow or complex and where quantitative PCR is really coming to its limits.

And this opens up important applications. doesn't it?

Yes. For example, in oncology, the QIAcuity-DX is used to monitor minimal residual disease, where you're looking for very small signals to help guide treatment decisions. This is where digital PCR can really make a difference to make fast, high-quality measurements that support decision-making.

So this is how QIAcuity digital PCR is used today across research and clinical applications. Thank you, Huw. Thank you, Francesca. QIAcuity digital PCR combines precision, reproducibility and ease of use across a broad range of applications. But what does it mean in a real clinical setting. Let's hear from our customer, Sean Monahan from Brown University Health, who is tackling one of the most critical challenges in health care. Sepsis. He's going to tell us more about how QIAcuity digital PCR is supporting decision-making in a clinical environment.

As a trauma and critical care surgeon at Rhode Island Hospital, I spent much of my clinical work hearing for very, very low patients. My research is [indiscernible] understand sepsis as a definitive diagnosis of that infection can take days. And you have this [indiscernible] period where you think the patient may have sepsis but you don't know for sure, so you give them [indiscernible] antibiotics and hope that they improve. The issue is that every delay in appropriate antibiotics for those patients, we have an increase in our mortality rate. In my research lab, we have been studying RNA sequencing data from sepsis patients for about 7 to 8 years. We identified a method where we could identify RNA from pathogens of interests that are causing the infections.

However, we knew we couldn't wait the days to weeks that takes for RNA sequencing data to come back for this to have it. We decided to translate or transition to a digital PCR machine, and that's where we decided to use the QIAcuity-DX with a QIAcuity-DX digital PCR in general, is that we're able to get this level or copies per microliter for those pathogens.

With this level, it's no longer just say yes, no. Instead, we have a level that can correlate with the patients' outcomes. When we get a sample from the patient, we can go from sample to result in about 5 hours. We know that with the QIAcuity-DX, we have a very high sensitivity down to 5 copies per microliter, which is very small amount. I would have to say the most beneficial aspect of the QIAcuity-DX for us is having this level of the result for the PCR that's very different from QPCR or any other really molecular techniques that are out there.

And in our research, we're able to show that those copies from regulator have correlated with different clinical outcomes such as whether the patient can be discharged from the ER to the home and the patient as to the ICU or even if the treatment is working. The QIAcuity-DX has allowed us to make our process from sample to actual moment much quicker with the QIAcuity-DX we have a process where there are a few touch points with a faster diagnosis will be able to tailor those antibiotics directly to those patients so that we don't have to use multiple antibiotics and we can narrow it down to 1 and see if that antibiotics are working.

We've explored the QIAcuity technology, some applications and customer use cases. Now let's have a closer look into the business perspective. And with that, let me hand over to Nitin Sood, our Head of Product Portfolio and Innovation and Fernando Beils, our Head of Global Commercial Operations.

Digital PCR is one of the fastest-growing areas of molecular testing and QIAGEN's QIAcuity is designed to make this technology more accessible. QIAcuity bridges the gap between traditional QPCR and NGS. It has the sensitivity and accuracy of NGS and combines it with the speed and simplicity of QPCR.

The digital PCR market itself is $600 million and growing robustly at 15% CAGR through 2028. In addition, there are opportunities to convert selected applications out of the NGS market applications that require less number of targets. On top of that, we have the QPCR market and applications in there that can be converted to digital PCR that require more sensitivity and more accuracy.

We're executing against our growth strategies and seeing strong momentum across the business. In 2025, we did $89 million in revenue and are expecting to do about $100 million in revenue in 2026. We're winning because we are the easiest platform we use on the market. QIAcuity's workflow is as simple as that of traditional QPCR workflows. We also win because we cover low throughput labs and high throughput labs. And we cover a wide variety of applications in life sciences as well as in diagnostics.

And lastly, we're making inroads into gene expression, the single largest application for traditional QPCR. Since we launched QIAcuity in 2020, we have focused on serving a broad range of customers and applications. For our academic customers or customers that are just starting out with digital PCR, we have QIAcuity1, which serves one plate. As our customers scale their applications, particularly in translational research or in biopharma or in clinical diagnostic labs, we have QIAcuity 4 and QIAcuity 8, serving 4 and 8 plates.

To support a wide variety of applications, we provide more than 2,700 QIAcuity digital PCR assays. In addition, if customers have need for novel applications or assays. We provide GeneGlobe where they can easily design new assays.

All these applications have resulted in over 1,100 publications that reference QIAcuity in 2025.

Our momentum in digital PCR is clearly driven by differentiation with an installed base of more than 3,200 systems, which is a CAGR of 75% and also as a result, we had a revenue CAGR of 55%. And this differentiation is clearly visible. One of the attractive unique selling points in our digital PCR solution is the throughput today 1,500 samples per day, we can process, thanks to the variety and the scalability of our platform.

At the same time, our multiplexing capabilities are continuing to increase so that we're able to test up to 12 targets in one single reaction. That differentiation is not only about performance metrics. What also matters is the feedback of our customers. From food testing to biopharma to wastewater testing, digital PCR represents, and this is a customer feedback, the next generation of PCR testing.

What we achieved with all our engineers across these years with the breadth of the portfolio was to make it as easy as QPCR. QIAcuity is part of a larger ecosystem, which serves from R&D down to quality control. And I had the opportunity to meet a large biopharma customer who was using our QIAcuity DPCR solution and viral sector analysis. And this enabled them to apply our digital PCR solution, QIAcuity from sample to insight. This is where we come in as QIAGEN. And this is also our offering, how we can enable our customers to grow, and we can customize the solutions for their needs from quality control down to research and development.

And this is another example on how QIAGEN expands and grow customer relationships across applications and workflows. One of the biggest opportunities for QIAcuity is gene expression, the single largest application within the $2.7 billion QPCR market.

What is gene expression? Gene expression is a foundational tool in disease biology that measures which genes are turned on and which genes are turned off. QIAcuity builds on the strength of QPCR and the fact that it's easy to use and it's fast but it overcomes the limitations of QPCR by being more sensitive by being more accurate and more reproducible, allowing researchers to uncover disease-specific gene expression signals that QPCR may miss.

In 2025, there were over 17,000 publications in gene expression. And this number is growing by 35% annually. To serve this very important market, we're launching a series of products. First, we're launching assays in mouse, rat and humans. In addition, we're launching the high multiplex mix that allows our customers to interrogate 12 targets in 1 reaction.

Our new solutions will enable researchers to detect subtle changes in gene expression and their high sensitivity will enable researchers to find the needle in a haystack. When customers work with QIAcuity, they get access to the breadth and flexibility of our assay ecosystem. Customers can go to GeneGlobe our assay design platform where they can gain access to 10 million predesigned assays and unlimited customization abilities.

We as QIAGEN, we achieved to bring the simplicity, the control into digital PCR and the ease of use, the adoption, the scalability, the capability of multiplexing, you get this all in that platform. furthermore, expanding into Gene expression furthermore into expanding into other applications, be it in the clinical field, be it in life science, be it in applied, be it in translational QIAcuity digital PCR solution is covering this breadth of the field.

It is designed with the customer in mind across all these segments. And furthermore, we are stepping into companion diagnostics.

We at QIAGEN believe in digital PCR, one of the fastest-growing markets in molecular testing and our QIAcuity platform is leading this market. QIAcuity ease of use and performance wins the customer. Its scale keeps them and our continuous innovation expands our customer base. With the QIAcuity Equity ecosystem, we're well positioned for future growth.

Thank you, Nitin and Fernando. We now know what QIAcuity is all about. But there is 1 important aspect of our QIAcuity story that we haven't touched today, and this is our pharma partnerships. Before my colleague, Huw went into his digital PCR role, he was part of the companion diagnostics team. And he had the chance to talk to Jonathan Arnold, Head of partnering for precision diagnostics and Richard Watts from the business development for companion diagnostics team. Over to you.

Okay. Thank you, Domenica. Jonathan, let's start simply. For those who are not familiar with the topic, what is a companion diagnostic? And why is it needed?

Sure. Thanks, Huw. Great question. And I would probably take it from a -- let's take it from a patient clinician perspective. At the most basic level, what I consider a companion diagnostic is essentially a patient has been diagnosed with cancer typically.

Physician has assessed that patient is make it a determination about therapies and essentially needs to diagnostic to determine if it's -- if the patient is eligible for the therapy. And so to me, this is the perfect example of precision medicine, finding the right patient with the right drug at the right time.

Well, from a pharma perspective, so they're running a therapeutic program. They've developed a drug the clinician is making a determination about what drug is right for the patient ultimately. And essentially, the pharmaceutical partner is going to have to invest in the diagnostic to ensure that we are selecting the right patients. And so the pharmaceutical company really needs a partner that they can trust that has the competency capabilities to develop the diagnostic because without the diagnostic, there is no drug prescription.

Where does QIAGEN come in? And what's your role in the process?

So QIAGEN really acts as a trusted partner, and we are that partner because of our competence across the requirements that pharma needs. So if you think about our leadership in PCR technologies, both QPCR and DPCR and the CAD is really resonating with pharma. We also have more than 30 mass collaboration agreements with global pharmaceutical companies. And this is important because it really establishes as repeat customers. And this is what I take most pride in, not just the absolute number. but it signifies that these partners trust us and they want to do repeat business with this.

So I think when people first look at companion diagnostics, they often think about developing the test as you've described there and just getting paid for that from pharmaceutical companies. But is that really the right way to be thinking about it?

Well, it's true that essentially, we are a commercial contract development business. So they are paying us to develop the diagnostics, which is great. It's a very important business to us. But that's not really what I think about the strategic value of our precision diagnostic businesses to CIG. The strategic value of our precision diagnostic business is developing innovative differentiated content for QIAGEN platforms. And so the pharmaceutical companies are engaging with us to develop these novel innovative diagnostics. We own the diagnostic we then launch it on to QIAGEN platforms, especially the QIAcuity DX. And this, in turn, make those platforms more attractive. So it's a very virtuous cycle. So we're launching novel content that no other company typically has access to, which then makes our instruments more attractive to our customers.

It sounds like you're working with a broad range of pharma partners. How should we think about QIAGEN's position within the space today?

So I think of it, we really have a leadership position. We've been doing this for a long time. As I mentioned, those 14 PMAs over roughly the last dedicate is testimony to that. Companion diagnostics is a tough business. If you think about these programs that we're supporting for our pharmaceutical partners, they're often billion-dollar programs. And so really, that concept of our risk is their risk and vice versa. We take very seriously. But we execute on time where we make commitments to these partners, we deliver.

I guess there's been recent interest in the field of ESR1, for example, as a biomarker, a companion diagnostic biomarker.

Maybe Richard, could you explain why that is?

Yes. Sure, Huw. So in breast cancer, ESR1 mutation in the estrogen receptor endocrine therapy. It is a key therapy that delays the progression of disease. Endocrine therapy is a treatment such as aromatase inhibitors. Those robots inhibitors do a great job but over time, patients start to develop resistance and progress the disease. With ESR1 mutations progressing this disease, the biology isn't detectable in the image.

And so is ESR1 mutation status needs to be characterized at the molecular level.

And how does this play out in the patient journey that explain a little bit.

So if a patient is diagnosed as I mentioned, with HR-positive, ER positive breast cancer, then that patient is given endocrine therapy.

And then the patient is then monitored on a 6- to 12-month basis. It is when that patient starts to progress when we start to see the disease developing resistance that we need to check to see if the ESR1 mutation is present or not. And that's where QIAGEN can step in with decentralized testing at the local level to help the oncologists make treatment decisions based upon analyzing blood samples taken from patients to determine if the ESR1 mutation is present.

How could a acuity digital PCR be good for ESR1 blood testing?

So the QIAcuity DX and the application of digital PCR is really a magnifying glass to the molecular pathology world. It really allows us to go exquisitely sensitive into the analysis of the circulating tumor DNA that could be present in that patient's blood sample.

So that's how it works today, how CDX is working today. Where do you see this evolving going forward?

Well, the analysis of circulating tumor DNA is really a paradigm shift in oncology and treatment decision making. We're looking for the detection of what we call minimal residual disease. The application of digital PCR is being applied in conjunction with next-generation sequencing towards MRD detection generally speaking. So it's a paradigm shift that's opening a new form of treatment that can be given to patients to extend their life.

So maybe going back to you, Jonathan, beyond oncology, how far do you think this model could extend?

Sure. No, great question. And it's one thing that I think of our companion diagnostic business at QIAGEN as so much of a platform. So it allows us to look into the future. So I often say, we don't have to be smart. We just have to follow the money.

And so we're able to see where pharma is investing biomarkers, technologies. And if you think about how we apply that, this is what I mean by innovative testing.

We're always ahead of the curve because pharma is looking across the horizon as well.

And so in partnership with and we see these things, they basically contract with pharma or with QIAGEN to develop them and then we launched them on these platforms. And so I really think of our CDx business as a platform enabling QIAGEN instruments and consumables.

Fantastic. Thanks very much, Jonathan. Thanks, Richard. Thank you, Jonathan and Richard. This is clearly an exciting opportunity for our QIAcuity digital PCR. Now let's hear from our CEO, Thierry Bernard and how QIAcuity is positioned for future growth.

Thank you, Dominica, and good afternoon to everybody. I have 2 key messages. You have seen Nitin and Fernando presenting the value of our solution, QIAcuity. You have seen multiple testimonies from customers. Research, companion diagnostic, but also clinical customers.

My 2 key messages are very simple. First, digital PCR at QIAGEN or digital PCR by QIAGEN is not just a technology anymore. It's a full ecosystem, a sustainable ecosystem where QIAGEN fully masters the instrumentation, the consumable, the reagents, applications menu and the bioinformatics.

Second, we are just at the beginning of what we believe to be a revolution in molecular biology, digital PCR. We believe that QIAGEN is already a leader but we want to continue that leadership and continue to invest to provide everyday more solutions to our customers, be them research, academia, pharmaceutical companies or clinical labs.

If you think about it, what do customers want today?

First, they want reproducibility. Second, -- they want scalability. And third, they want to be able to detect more pathogens into one single sample simultaneously. Many companies are able to provide customers with reproducibility, with scalability with multiplexing.

But there is something also very important that customers want. It's simplicity. And I think it's fair to say that QIAGEN is the only company to be able to offer and provide customers with reproducibility, scalability, multiplexing, but also simplicity Digital PC but QIAGEN, as you have heard from Nitin, from our customers and from Fernando, it's one sample in and the result out.

It's a fully integrated box. So this unique feature of digital PCR by QIAGEN of QIAcuity translating numbers today. You got it. We launched it roughly 4 years ago. In 4 years, we took more than 12% of an estimated market already at $600 million. More than 3,200 systems placed since we launched that solution.

1,100 publication to support the value of QIAcuity. This is probably unprecedented. We are already the #2 in this market, and we are on our way to become the clear number one. But there is no way we are going to stand still, and we want to continue to invest to enhance that leadership. And I see 3 ways or 3 priorities for those investments.

First, obviously, continue to increase the potential applications available for customers. We started with a lot of application at the beginning for research and academia. We extended it to pharma companies, but we want to move also to new fields. Think about human identifications; forensics. Second, companion diagnostic is probably one of the major growth field for QIAcuity and digital PCR. We are extremely well placed at QIAGEN because we already can leverage more than 30 pharma partnerships to push that solution to our pharma partners. And the third major investment for our company in the month, the weeks, the years to come, is to be the leader converting the gene expression market into digital PCR.

Gene expression is probably one of the major applications in QPCR today all over the world. But think about it, customers will continue to look for more targets for speed, for accuracy, but in a simple workflow. QIAcuity is ideally positioned to answer those needs. I'm not saying that tomorrow digital PCR, we fully replace QPCR, that's not the point. And by the way, digital PCR will not fully replace next-generation sequencing either, but see it that way.

Digital PCR is allowing our customers to find more targets in 1 samples in a fast way than traditional QPCR, and this is very important, without the complexity of next-generation sequencing. And so when I think about QIAcuity for the future, I see a double-digit growth potential for our company. I see QIAGEN clearly taking the lead in this market.

I see QIAGEN clearly converting more and more QPC application into digital PCR. I see QIAcuity leading the move of PCR in gene expression for QPCR to digital PCR. And I see it as a very major investment for our company. And now back to you, Dominica.

Thank you, Thierry. Before moving on to the Q&A, we're happy to share more customer voices and their experiences with the QIAcuity.

My name is Paul Ramachandran, and I'm the CFO and Co-Founder and Tracey Bio. For decades, imaging has been the mainstay of how we monitor cancer patients minimal residual disease is an attempt to go beyond that and measure microscopic amounts of in patient blood that are not detectable by imaging.

This allows us to more quickly assess whether a patient is responding to therapy when we need to switch therapies and catch recurrence much, much earlier. At the large point stream of MRD, we want to be able to detect a single molecule from the tumor in a blood sample from a patient.

This requires every step in the process to be perfect. From sample collection to DNA extraction and then ultimately, detection of that single molecule using digital PCR. When we first started working with the QIAcuity, we, I think, like many others, so QIAGEN is the maker of kits that come in blue boxes and reagents. When we started a race it would take one technician, a ton of manual work, what that meant was it would take them approximately day to build an assay for a single mutation for a single patient.

But the simplicity of the QIAcuity workflow, we've been able to automate all the pieces around this. Now the technician doesn't have to do any of the work. It's all done [indiscernible] and the robot can build assays for 10 different mutations for 20 minutes. This has yielded greater than 100x speed up in our workflow.

I'm an associate professor at Florida State University. My lab works on developing methods which can reliably test for presence of Salmonella in poultry presence of E.coli in red meat samples so that the companies can reproducibly test their food and protect people. I started working on digital PCR assays in 2023 was having a conversation with the stakeholders that we don't need to only do presence and testing of salmonella.

We also need to count how many salmonella cells are present in the food -- if they have a higher salmonella load in the fluid sample that product should be also eliminated or stock from entering the comp working on food samples for the last 10, 15 years, I know that relative quantification will be always challenging the food samples because food samples are high in protein high in fat and high in all PCR inhibitors you can think of.

And that's why I chose DPCR for quantifying salmonella and whole cell samples. What I value most about the QIAcuity digital PCR platform the one unit does everything from partitioning the plates, doing the PCR and also imaging the plate. Everything done in one box. Second part, it quantifies this presence of target DNA. I also very much appreciate its ability to co-detect to or more targets in within 1 sell of that period.

Thanks, Gopal and [indiscernible] You've seen today 3 customer voices. And we've prepared 3 more for you, which you can see after the deep dive on our web page coming from Novartis, Bristol Myers Squibb, and Zalaris..

Now we come to the last point of our session today, which is the Q&A and if you haven't done. [Operator Instructions] Today, together joining the Q&A session with me in the studio are Daniel Wendorff and Huw Ricketts . Welcome and we also have more speakers for today's Q&A that you can see on the screen, which are Thierry Bernard, Nitin Sood, Fernando Beils and Jonathan Arnold.

Perfect. Thanks a lot. I think we're ready with the first question, Daniel.

Yes. So the first question is what differentiates QIAcuity most strongly when customers evaluate competing digital PCR platforms.

Well, I think we can be several of us. When we launched QIAcuity 4 years ago, the main differentiation were coming from the -- was coming from the simplicity. I mean it was the first time that the company was launching a digital PCR system fully integrated, 1 box, sampling, result out. And this for 3 kinds of different throughputs.

And clearly, in the recent years, some competitors have tried to also integrate their solution. But our plate based technology makes it simpler and much more cost-efficient than any other competitive solution at the moment in the market. And this is why notably on the American market, anytime we are faced with competition. Our heat rate is above 70%. That's quite remarkable. Nitin or Huw if you want to complete that differentiation.

Yes.

I mean I think I'd add a couple of points, Thierry. One is that in addition to being much easier to use. It's one platform that scales from 1 play to 8. So when a user gets used to our software, our ecosystem, they can very easily scale and the second is that scalability extends from research all the way to diagnostics. So they can start out on our research use platforms and as they move into the diagnostic application, they can use the DX platform, again, the same underlying technology platform, same software.

And then lastly, we have the GeneGlobe ecosystem where there are tens of millions of assays to choose from lots of customizability available to our customers and then 2,700 validated assays for them to pick from. Anything to add, Huw?

I think you've captured everything there and in it, and I think I can't add anything else. It's perfect.

Perfect. Let's go to the next one, which is you mentioned that customers are increasingly switching to digital PCR where in that transition curve are we? And do we expect the majority of our QPCR installed base to switch to digital PCR? Or will we have customers that use both Q and DPCR.

I think we need to be very clear here. QIAGEN in many different situation has repeatedly said, cannibalization is not what is going to happen. Digital PCR is not going to fully cannibalize total. Digital PCR is not going to fully cannibalize next generation sequencing either. But by combining the fact that we are giving more answers with digital PCR than with QPCR, without the complexity of next generation sequencing and the turn to result of next-generation sequencing, we have created a new need.

So we are also opening new frontiers from our customers, be them pharma company, clinical lab research and academia. So there will be some conversion, obviously, on both sides, both from QPCR and also from engines, but it's not purely cannibalization. For us, as we said in the presentation, 1 of the major potential for conversion will be around gene expression.

We all know that gene expression is one of the key markets currently in QPCR with that all the market in expression will move to digital PCR no, clearly, but we want to convert a big partner. As for the transition from our own portfolio, to digital PCR. It's very fair to say that in the coming years, QIAGEN will invest much more in digital PCR than in QPCR. But what is important is that being a leader in molecular biology. As of today, QIAGEN is the only company in the market to offer valid solutions in QPCR, in digital PCR and in next-generation and to offer those solutions both to research, academia, clinical customers, pharma and many other applications.

Perfect. So let's take one on clinical and then we move on to gene expression. So can you speak about some more of the applications in the clinical setting that we see our customers moving to digital PCR and what are the fastest-growing areas of the clinical market and which applications do we think provides the biggest opportunity for us.

It's a market in the making, but Huw you might want to take this one. And also what we presented today in companion diagnostic is a good answer .

Yes. Thank you very much, Thierry. Absolutely. It's a great question. And we see -- we do see an expansion in clinical applications, anything where you may want to take repeated time points, samples of the repeated time points. for example, the ESR 1 example Richard talked to us about, that's classically strong for digital PCR. You get the precision in the measurements between time points is a critical point. So anything in that oncology space is going to be important for clinical applications, but also something like transplants. We're seeing quite a lot of opportunities in transplant monitoring of patients who have had a transplant.

Daniel, do you want to continue with gene expression?

Yes. One question which came quite often is how important really is gene expression as a future growth driver for the QIAcuity platform.

I think Nitin could give some indications here.

Yes. Gene expression is a really important market, as you heard in the presentation 30,000 publications in gene expression growing at 35% year-over-year. So it continues to be an extremely important tool in analysis of diseases. And where QIAcuity shine is finding the needle in the haystack, finding the gene expression signals the traditional QPCR will miss.

And that's going to uncover more disease biology to help obviously develop better diagnostics and better drugs. Today, 10% of our instruments go into gene expression and with the launch of new kits that we just announced, we expect that to increase.

And then we're not just stopping there. You've heard us say we're launching -- working on our second generation platform, and that will further accelerate the penetration into the gene expression market. It's a very important market.

Perfect. And we have one on the EUR 600 million total addressable market in 2025. How much of that was clinical versus research and also similarly for our growth outlook through 2028. How is the break between clinical and research.

The majority of the market is still in research and academia. As we said, the clinical market is in the making and QIAGEN strategy is to boost that evolution via our [indiscernible] companies partners and our companion diagnostics. But it also, for us, the strategy is to put that technology in the hands of as many applications and customers as possible. You saw the example [indiscernible] for example, is developing is [indiscernible] approach in Rhode Island and thanks to our technology, what is developing it, we are supporting, obviously, but there are many applications that this way we want to push customers in HID, in forensics, in agri business, in food control, for example, to try that technology because we know it brings value. So it's fair to say that the market is probably at the moment, still 70%, 60% to 70% Research academia, but the clinical applications are moving fast.

Yes. We have one more question. What are the biggest barriers preventing broader conversion from quantitative PCR to digital PCR today?

Huw as the Head of Marketing, would you want to take that.

Pleasure. Thanks,. I think in the past, many customers were, let's say, fearful of digital PCR because of the difficulty with the workflow. It's a challenging workflow with the QIAcuity that's gone now. It's an ease of use. It's just like key PCR. You're using a plate-based system, you're setting up basically a key PCR reaction using digital PCR. So I expect customers will adopt this because of the ease of use.

Okay. Perfect. Then I would say let's move to companion diagnostics. And what's the real status of the 3 partnerships for the QIAcuity CDx?

Sure. So I can't comment directly on any individual program. These are highly confidential for our partners. But I can confidently say they're on track. We're expecting launches in the next 12 to 24 months. It's always hard to precise a time line because essentially, we're married to the clinical time lines as well for the therapeutic.

I'm also very, very bullish on our pipeline as I see the progression of digital PCR into our pipeline with farmers in the medium term, it will be the primary technology for our companion diagnostic business. So things are going very well on the companion diagnostic side. Pharma understands and appreciates the value proposition of the QIAcuity DX as we look at those monitoring applications, we see it as a nice complement to NGS. NGS will always be the primary diagnostic in my mind for oncology. But there's other applications where it's not the best, and we see that's where DPCR is resonating right now. So things are good.

Yes, I have 1 more. where within the approximately $2.7 billion PCR market, do you see the greatest opportunity for digital PCR conversion.

Fernando, Nitin, you want to come back to this one?

Yes. I mean, I think we talked about this. We expect, again, the gene expression market, which is about 50% of that $2.7 billion market to be the most exciting opportunity. But broadly, wherever you require high sensitivity, accuracy, precision and you want to do repeat monitoring we expect digital PCR to make inroads into the QPCR market. Fernando, anything to add?

Easy for our future customers for regards to reproducibility easiness, multiplex, you heard up to 12 targets, which is coming up. And on top of this, more than 2,700 assays available and the large liability of customization opportunities. So we want make it easy for our customers and future customers to convert pretty easily.

Perfect. Then let's give additional color on the revenue mix across different applications, gene expression, cell and gene therapy, liquid biopsies, mentioned, quality control and so on but also on end customers, academia, the clinical field, where are we with that conversion?

Well, first, I think -- the first thing I'm going to highlight is that digital PCR QIAcuity is clearly 1 of our pillars in growth. As a result, basically also received one of our highest investment into research and development. We have dedicated people on the field, who are [indiscernible] digital PCR. We have a dedicated team for companion diagnostic who's focusing also on pushing this technology to our pharmas.

So you know the numbers, Nitin has given you the numbers for 2025, the target for 2026 as well. We are not splitting those numbers into clinical or research academia or into gene expression, QPCR and so on. What is clear, the key messages are the following. Since we launched this QCPR we have developed the number of applications to fuel that go. We started for research and academia, and we also to sell and gene therapy and move to also QPCR control. We are now moving into gene expression in the second half of 2026. Since the launch of QIAcuity, again, at the beginning, research and academia [indiscernible].

We brought that solution to regulatory authorities, IVDR, FDA, we blow that solution to our pharma apartments. That's how we invite you to see. We have a target which is to become the #1 in this growing market. We see digital PCL at a double-digit growth product in our portfolio. .

This market is growing. We have a good solution. We have a different differentiated solution. We have a cost-efficient solution. We have people dedicated to market it and nearly, as I said, many, we will be #1 in digital PCR. And if we don't, it won't be because of the so. It's because of management, I would say. It's just a matter of execution [indiscernible]

Perfect. And we have a couple of questions on conversion NGS to digital PCR. So can we talk about -- more about digital PCR when digital PCR would be used over a next-generation sequencing particularly as in the oncology space. So when you can get more genetic information from NGS alone by going with digital PCR and if not completely used over NGS specifically, how is this used in a tandem with NGS?

Insisting again on the fact that it's not about cannibalization, but providing customers with a new divided solution. I will invite who are needing to take that question.

But again, it's not about cannibalization. It's basically bringing value compared to what NGS brings to clinicians and patients and compared to what QCPR brings to clinician and patient.

Absolutely. Thanks, [indiscernible] And you hear from Jonathan as well. In oncology, NGS is going to be the primary diagnostics most of time. where we see, as Thierry said, digital PCR is a complement to NGS. And actually, often they're combined together to give more information -- in onco-hematology, we see a lot of digital PCR being used because often onco-hematology is defined by a small subset of genomic alterations.

So you don't necessarily always need NGS, and you might need speed to these patients are extremely sick in an answer quickly. So digital PCR fits very nicely there.

On the Hamilton integration, what percentage of customers would benefit from Hamilton integration and what are good examples of potential use cases.

Nitin, do you want to take this one? .

Yes. So one of the primary applications we are targeting with this integration is really in the cell and gene therapy QC space. As our customers are moving from sort of method development and moving digital PCR from that space into QC of released drugs, they need higher throughput.

And as a result, they will benefit from automation and higher scale. And likewise, as we scale out our customers are scaling out in applied testing as well as in clinical diagnostics. Those are another category of customers that would benefit from more automation.

And we have time for one more, I guess. What products are you launching to target gene expression in the second half of 2016 and already 10% of instruments today? So what's changing?

Nitin on the assays that we are going to launch in the second half of the year?

So we're launching 2 categories of assays for us, as you heard, we are launching panels that target various pathways in mouse, rat and in human. These are miles on ramping motor organisms and of course, human being a very important category. And then we're launching the one-step 12 for multiplex in kit and gene expression. One step, meaning you will be able to do a generation of CDNA from RNA and amplification in one step in the instrument itself is making the workflow simpler and I just want to remind everyone that at QIAGEN, we also have our bioinformatics solutions, our IDA, which does pathway analysis, which also contains the latest greatest information about the new pathways that arenas covered.

So we'll continuously add new pathway specific gene expression panels.

And so that's going to drive growth. And then as I've mentioned, we continue to innovate, and we have more things in the pipeline that will help us [indiscernible] penetration gene expression.

And with that, we are almost at the end. Before closing the session, I would like to hand over for some final remarks.

Yes, well. Thanks again all of you for your attention night. Continue to be did, I hope that you appreciate this format of one hour investor relation and deep dive. I would like to thank Domenica and the team for the preparation of this event. Obviously, we remain open to your questions if you are questioned by Email. The final message for me would be very simple.

For a molecular biology company like QIAGEN moving into digital PCR was clearly a natural step. What we have executed have achieved over the last 4 years is nothing short of remarkable. It is probably the fastest growth of an installed base in tools, life science and diagnostics achieving more than system is such a quick time is remarkable.

But as Nitin said, Jonathan and Huw said, we don't want to stand still already in our pipeline is a new instrument. We could leave at the moment QIAcuity version 2 or generation to. Obviously, we will update you as we go, but see that investment are a clear proof that one QIAGEN is definitely a digital PCR company; and two, that we are going to fuel our ambition to convert the market of QPCR. And any time we can also the market of NGS to this new technology. Thank you, and talk to you soon. Thank you.

Thank you. And with that, we are at the end of the QIAcuity deep dive session. Thanks for your participation and for all the questions that we received. And with that, have a great day. And if you have any further questions, always feel free to reach out to us. Happy to help and see you then. Bye-bye.

Okay. We're going to kick it off. I'm Tycho Peterson from the life science team. It's my pleasure to introduce QIAGEN. We've got Roland with us today. Let's jump into it. And maybe setting the stage here, just talking a little bit about trends coming out of 1Q. You had the guidance reset. Just start at a high level, how should we be thinking about what was kind of idiosyncratic in the quarter and broader demand trends as you feel about the rest of the year?

[indiscernible], so which is probably more important. But I think you're absolutely right. I think overall, the Q1 start of the year was, I would say, a quarter with mixed results. On one side, 4 of our 5 growth drivers actually performed quite well. At the same time, QuantiFERON clearly had a difficult start that was due to the immigration-based testing, particularly in the U.S.

Just to remind you, QuantiFERON for us is about a $500 million business for us. 10% of that is immigration-based testing. By far, the majority is legal immigration. And one thing that we clearly had to experience is that there were changes coming up in the legislation in the U.S. took some time that they got effective. We really haven't seen any larger changes more or less all the way through February of this year.

But then digging into that, it became quite obvious that some of our larger clients have seen that impact. Have in mind that kind of testing is not done in any kind of dedicated lab environment. It is done with a very regular centralized labs and that probably also took them some time to figure that out and to rebalancing. Nevertheless, what we did is we took literally 100% of the exposure in the U.S. out, which is around USD 30 million.

At the same time, of course, we see similar trends for very different reasons in the Middle East. We might go back a couple of years when we clearly talked about that, that we won the TB testing in areas like Qatar, Dubai, Abu Dhabi and so on. Given for the war, we also took out $5 million for that. We haven't seen any change in Europe for immigration-based testing, nor have we seen any change in 90% of the TB business. And therefore, I think that is quite stable.

Now being in Q2, I would say what we did was the right thing. I think trends got confirmed. So if you go back to the call what we said, we said QuantiFERON around minus 5% in Q1. Probably Q2 is flattish, slightly negative. Q3 is slightly positive and Q4 more or less a normalized growth rate. I do think that is what we also see today and therefore, no change.

Of course, as we had to know going also to your second part, given the changes we have seen then and realized on QuantiFERON, of course, we turned a lot of other stores within the company. That's also the reason why we took a couple of larger OEM deals out of the guidance because the one thing is very clear, we delivered until Q1, 26 quarters in a row in terms of revenues and in terms of EPS. Once you realize, you have to reset guidance for a specific reason, you turn every other stone.

And we'll jump into the businesses in a minute. I guess before I do, I just want to hit on the CEO search. You kicked it off in November. Originally, we were targeting June, now kind of back half of the year. Just walk us through where we are in the process, how you're thinking about the candidates, how the Board is thinking about what the business needs at this stage?

Yes. No, I think it's fair to say in the last call, we updated it, that it is probably now more an H2 event. I don't think it will be all the way down to December, but it's clearly an H2 event. A couple of reasons for that. First of all, the Board is looking for what you probably would call in U.S. like somebody who has seen the movie. So a very senior experienced leader, clearly with a strong footprint in the life science and in the clinical side. Clearly, given also QIAGEN international setting, somebody who has either lived and worked in Europe and/or the U.S. So also here, somebody who's rather very experienced.

I don't think that you should, because of the "delay", read into that, that we are short of candidates. I think it's probably actually the opposite. But at the same time, as a lot of investors were waiting for clarity from some of the CMDs, one of our competitors had on the QuantiFERON product on the QIAGEN side. There's also other parties who are waiting for that kind of feedback, and that probably led to the situation and discussion. Let's wait a couple of more weeks.

And anything you can say about what the Board is looking for? I mean you mentioned international and -- but...

Again, senior person, C-level experience. Again, somebody who did the job in a different country before.

Let's jump in on QuantiFERON, I guess, the biggest swing factor to the reset guidance, you've taken down expectations on immigration. Are we at a clean base from here? Or are there some moving pieces for the next couple of quarters?

It's about immigration. The rest -- it's very straightforward. It haven't really changed. Again, we are careful in taking out 100% of the exposure in U.S. I'm not sure that's 100% realistic. At the same time, we do not expect any legislation change in the U.S. as well. Therefore, I think it's the right thing to do.

In the Middle East, I would call it that at some point, either the war is going to end or we will see these countries going back into -- going back to a more normalized environment like we see that in [indiscernible] and others, so back to work, if you like. The reason for that is -- and therefore, I think there, we should see again some normalization. It's hard to say when, but for sure, will not take us long.

And just how about underlying growth ex immigration? What did that look like in the first quarter? How do you think about that for the remainder of '26?

As you know, overall, we said it a kind of a 6% growth rate for the full year. Now of course, we took $35 million out of that number. So end of the year, we will grow again that business nicely single digits and let you exactly where we are.

You mentioned the competitive dynamic. I guess what we saw there was limited markers, limited head-to-head data on sensitivity specificity, lingering questions on workflow. You've obviously laid out your road map on automation with the Inpeco partnership. Just talk a little bit about how you're thinking about competitive dynamics evolving and with the market obviously getting ahead of itself relatively to the headwinds?

Yes, I think it's probably a fair summary. I do think that will get you a couple of remarkable outcomes. First and foremost, as you were alluding to it, it looks like that our competitor is missing one very important critical market, which is CD4/CD8. Why is CD4/CD8 so important? That is for the subsegment, which is actually the fastest-growing subsegment if it comes to latent TB testing, immunocompromised patients, the critical marker. If you don't have that, it's hard to test.

And I do think that is important, again, and clearly a factor also for the labs because depending a bit on where you are in the world, it is a population group between 10% and 20% of the total population and the testing population. And of course, as I said, the fastest-growing population as well. So I'm not sure that you will see customers going for 2 different work streams to address that topic.

Second, it can be very clear that the automation solution, I think they said is beyond '28, a bit surprised by the wording. Typically, if I mean beyond '28, I would say '29. So I'm not sure what beyond '28 means. Very clear also that there's nothing short term in the U.S. We like the fact that they finally come up to the market in Europe because it's helpful for us to prove what we said before in terms of, again, our success in the market. So I think overall, I think it was incremental good news for QIAGEN, I would say.

And just on your pipeline, can you talk to the partnership changes with Inpeco and whether this should be viewed as shared defense, new lab adoption, potentially both?

I think Inpeco is a great addition to our overall workforce. We have a great partnership with DiaSorin on the back end that's not going to change. But on the front end, of course, there's a couple of steps which still require certain manual steps, which we are, of course, going to automate with the Inpeco solution going forward or we fully automate that. And that is clearly unique then to QIAGEN. Nobody else can do that.

And Inpeco is clearly a well-known proven provider for this kind of workflow automation. As we do believe that TB testing is still a significant volume grower, have in mind, 60% of the global market is still literally 120-year-old skin test. And even that skin test market is growing 4%. We do believe that there is an increasing need for automation and therefore, the Inpeco solution, which at the end of the day provides you with a rollaway solution is a step in the right direction.

And then maybe just shifting over to life science. The other piece of the guidance cut there was just reset expectations, partially on the weaker A&G outlook here and then the OEM headwind. I guess between the 2, you said $35 million, $40 million headwind for the year. Can you unpack each piece relative to what the expectations were when you first laid out guidance in February?

To be honest, it's not too much. The general environment for academia and life science in the U.S. Here, we -- I think it's also fair to say that historically, also last year, QIAGEN had a reasonable consumable performance. Clearly, instrumentation business was for us, as for many other, a bit more volatile.

But what we did, as I said before, we looked particularly in the larger OEM contracts, which are also part of the life science business. And we have here a couple of contracts with large government organizations in the U.S., but also in South America, where given the political environment, we are not 100% sure that they will come up. They were very reliable customers for the last 3 years, always high single-digit million dollars of revenues. But if you do, for example, something like pandemic preparedness, you might have orders in hand, but you're not 100% sure that it comes in. In a situation where you have to make sure that the new guide you set out is more than reasonable, you adjust this.

And I guess was the reset more of a forecasting issue or demand deterioration?

I think it's probably also just to make sure that the forecast is realistic and therefore, I think well doable. And again, that's probably the base behind that. I would say, overall, the automation business was actually quite strong for us. We talked about that in the call, Tycho. As you know, Sample prep, for example, instrumentation was growing double digit. So hard to complain about that, right? And as I said, consumable in general is moving in the right direction.

There always a couple of pockets who can do better. PCR in general is something that we clearly probably will draw a bit more attention to. But in general, we clearly see an increased activity, particularly on demos in terms of requests for proposals on the academic side on instruments. Will all of that lead to more revenues instantly? Probably not. But do we see, I would say, a certain kind of refreshment of interest? Yes.

And then just honing in on U.S. A&G. Obviously, you've got a slight increase in the budget up 1%. You've got this multiyear budget dynamic that's impacting labs. I guess how would you describe the backdrop now? And do you think there's a chance we'll get a pickup as we go through the summer?

Just to frame it also with some numbers. So our more or less work from H1 to H2 only requires $5 million more incremental revenues coming from a better life science environment. If that is our issue, I'm fine, right? So we do assume it will improve, as I said, on the instrumentation side. I think the bigger step forward for us clearly comes also with some of the new launches, particularly in Sample prep. There, we do expect around about $20 million of incremental revenues given the size of instruments we are launching with QIAsprint and QIAsymphony and also, I would say, the visibility on pipeline and so on. I think there's -- I would say, so far, we feel quite good about that.

So I would say environment in Europe, life science is good. Horizon budget is distributed. We're seeing more and more budgets in the U.S. finally reaching the benches. Is everything perfect right now? Absolutely not. But do we see that people are clearly getting more interested, particularly on the instrumentation side, yes.

And then maybe just shifting over to pharma. It seems to be better for most in the industry. Just from a high level, how did it do in 1Q relative to expectations for you guys?

Pharma for QIAGEN has a couple of very specific driver, which make it quite successful for us. One is QIAcuity. Clearly, pharma is a big partner here in biopharma research, double-digit growth rate in consumable and instrument in Q1. Same is actually Parse acquisition. I think what we -- Parse, clearly an outstanding product offering by itself. Now with the acquisition of QIAGEN, the partnering with our global pharma teams helps them also to gain access to some of these larger accounts. And these are sizable deals. That's also the reason why we said we feel quite comfortable on the $40 million guide we have given for Parse. So I would say, in general, pharma is for us probably more on the positive side.

And then as we think about biotech, I mean, funding has been good, sentiment strongest since 2022. Where in the portfolio will you see it when that funding starts to convert to spending for SMidCap biotech?

Several reasons, of course. [ Basically ], we see also biotechs clearly, again, doing more lab work. I'm not sure if they all want to generate now AI-based data also. But there's clearly more fundamental lab work done and therefore, again, areas like sample prep are important. Again, biotech is not like the largest customer group for QIAGEN, but clearly incrementally be helpful. Other area is actually around bioinformatics. Also here, I think we see increasingly request. So I would say it's always good that finally, I think the funding is on the highest level since 2020. Let's keep on going.

You mentioned Sample tech a couple of times and the expectation for a 200 basis point uplift in the back half of the year. I guess -- what's happening now? Is it funnel conversion? Is it replacement detailing, competitive wins? Just talk a little bit about what you're actually seeing on the ground to give you confidence in that pickup.

The uplift is actually somewhere between 400 and 500 bps, but some of them is quite easy because 200 bps is just the headwind from the deconsolidation of NeuMoDx and Dialunox will disappear as of June 30. So it's just a technical impact, right? So that's the 200 basis points. 200 basis points, as you said correctly, it's coming from the new product launches, particularly QIAsprint and QIAsymphony.

So the good news is these instruments are launched in the market. The pipeline is building. There was not too much in Q1. There's still be only a few in Q2. But again, the pipeline for Q3 and Q4 looks good. So I think that is going to happen. Have in mind also that QIAsprint clearly is a brand-new instrument. So every instrument we sell is not only an instrumentation sales. It's clearly also generating incremental consumable pull-through is therefore, important.

Also on the QIAstat side, you know that there's new launches coming up. So blood culture is a big topic here as well. So I would say on the new product launch, it's good. Then we have another 50 bps of what we discussed before. We clearly do believe that QuantiFERON should get better in the second quarter compared to the first half -- sorry, in the second half compared to the first half. And last but not least, Parse, as it is still growing and kicking off, we will have $5 million more revenue in the second half compared to the first half, so another 50 bps there.

And I guess just thinking midterm on the Sample tech, I think you've sized it at 115,000 placements or greater than for the 3 instruments combined as the opportunity. A couple of points tailwind there. What would get you to do better than that?

I think -- one thing what we already discussed is clearly, it's always good if you have a more stable environment and people have the belief that they can plan mid and long term because consumable is something what you buy for your daily work at the end of the day, right? So I think that's also a reason why we actually had a very reasonable consumable business last year. While the environment was not the easiest one for many companies, we were still growing, right? We shouldn't forget that QIAGEN still has, again, historically outperformed the industry quite nicely.

Instrumentation, again, is different. I think the benefit we're having is that most of our instruments are rather with a price point between $35,000, $40,000. And even the QIAsprint [indiscernible] configuration, it's probably around $70,000, $75,000. I think it's reasonably priced. So we would believe if people believe that there's a midterm budget the year after and not everybody loses his job, are going to buy an instrument. More important is it is not only life science, right? We clearly see that the pharma guys are going for the efficient solutions. We see volume growth with some of our liquid biopsy customers who are significant customers for us. You have seen a couple of them just a minutes ago, right? So I do think there's opportunities for us to grow also by other companies doing quite well.

What percentage of Sample tech systems do you think go into clinical placements, the new systems?

I would say the share on Sample prep instrument is not much different than the global split up. So it's roughly half life science, half on the clinical side.

And then parts, you touched on -- I think you suggested potential upside to the $40 million target this year. What's changed since the initial deal in terms of where you're seeing upside?

So yes, the interest of specially pharma and translational space for single cell is going up. The tau therapeutics data set with 100 million cells is definitely a good proof point that you can scale with the Parse technology and on top also keep quality, that's an important factor. And also in general, we see a shift from bulk analysis into single cell, but the major driver here is the pharma part.

And competitively, I mean, how do you see that? Obviously, scale that acquired around the same time. I mean, how do you see kind of the competitive dynamic playing out?

So, I mean, the Parse technology is instrument-free. You named it perfectly right that scale would be the head-to-head comparison. And here, we're not seeing much. Just look at the revenues, right, $40 million for Parse that we expect or even more than that for 2026 and then a handful of million from scale.

It's also the reason why we doubled down on R&D, you might know. While the business is actually doing quite well and actually has healthy gross margins, we clearly put quite some dollars into R&D because we want to build the menu even much faster than the original Parse plan was. It's the reason why it is dilutive for this year, particularly in Q1 and Q2. But again, we do believe also it pays off quite quickly.

Maybe we can hit on digital PCR, strong growth there, over 20% in the quarter. One of the more compelling stories, I think, in the 5-pillar plan. I think people are still trying to get comfortable with what the longer-term outlook, looks like for that business. So can you just talk on how you think about that trajectory? I know you originally laid out a 25% CAGR at the Capital Markets Day, and it's been below that. But how do you think about that business improving from here?

First and foremost, we should remind ourselves, right, that 4 out of the 5 growth drivers, I think, overall on track. And probably more important, nothing has changed. Our $2 billion target for 2028 on the 5 pillar of growth hasn't changed. You're right that the composition of the mix might be different [indiscernible]. But I think the $2 billion are more than doable. I do think that is not -- that hasn't changed, and I don't think there's any reason that it should change.

Particular QIAcuity, I think it was fair to say that last year, we had always good double-digit growth on the consumable side, but the instrumentation environment in general was difficult, not only for us but for many companies. Despite the fact, it was very encouraging that Q1 had a very good start, double-digit growth rate, not only in the consumables as always, but also on the instrumentation side. And I do think we will not expect anything different for the second quarter. And again, for the full year, we feel on track as well.

I think what makes the difference for us is clearly also the investments we made on the consumable side. I would say, historically, for sure, we agree to that, most people would say that QIAGEN always had a better instrumentation solution. But at the beginning, we were clearly a bit short on menu. But with the investments we made over the last 2 years, and we continue to do this year in expanding menu and portfolio for digital PCR, we are probably more than head-to-head, right? I think we have even a certain advantage there. And I think that pays off.

We are not standing still here. Also here on that side, we're clearly pushing hard on the menu side because we do believe the transformation from qPCR into digital PCR is just the beginning. If sequencing is doing well, it's great news for digital PCR because you need validation, you need quality control. It is always most likely digital PCR step. So there's a lot of good reasons to believe that business continues to do well.

You mentioned on the 1Q call kind of a prioritization strategically of digital PCR over qPCR. Can you maybe just talk about what needs to be done to drive more of that transition? Is it workflow, cost per sample for the menu development that Roland mentioned?

Yes. So just as a teaser here, we also have a deep dive coming up on June 15 on QIAcuity. There you will learn more about that. But just a few words on that. So if you just look into the qPCR space, then you will see that a lot is coming from gene expression. And this is something that we also mentioned earlier this year that this is something that we want to continue focusing on. And here, what is important for that multiplex capability is always a big topic. And here, you saw that we're able to target 12 -- or to analyze 12 targets in just one reaction.

Ease of use is important because, as you know, qPCR is a very simple technology. And then how can you automate that? And this is all what QIAcuity can do. Cost per sample is, of course -- cost per experiment is going down, the more targets you can put into one reaction. That's an important factor. And the menu as Roland mentioned, to just catch as many applications as possible in the space.

Maybe we can hit on QDI and you've taken growth expectations down from double digit to something closer to mid-single digit this year. Just talk a little bit about how much of that is discovery research sluggishness and what specifically changed in the underlying demand environment versus prior expectations?

Yes. Overall, we feel very good about the business. We shouldn't forget that right now, we're still going through a SaaS transition. That means, again, typically historically, customers were buying rather upfront licensing deals for typically 3-plus year periods, now they're going for rather quarterly installments. Overall, I would say it's probably somebody more profitable for us, but clearly having a different revenue recognition event for us.

In general, it's quite obvious that the clinical part of that is an important one. We clearly see also now that, again, some of the AI components are being helpful with helping customers getting more volume done. Again, I'm not sure long term is rather a high single-digit or low double-digit business. I wouldn't differentiate here too much. But overall, it's a nicely profitable business for us, which is growing above average.

Okay. I mean you previously talked about 15% CAGR for longer term, but now you think high single, low double?

Let's see where it ends.

And then, I guess, QIAstat, you're pointing to a meaningful ramp there, right, double digit in the back half of the year. Just walk us through what needs to go...

Performance of QIAstat was also a good start in the year in terms of placements. We have healthy -- as you know, historically, we always said if you have a 150 placements in the quarter, it's a good quarter for us. We had that 4x last year. And I would expect it's also the kind of a run rate we should expect for this year on average.

Clearly, respiratory is in Q1, but also in Q2, we said that on the call as well, is a tough comp. I think it's going to normalize in the second half. And we should also not forget that, again, as we said before, there's clearly an important launch coming for us. So we'll see how quickly that involves and contributes. But the significant ramp still comes from the launches of gastro and meningitis in the U.S. because have in mind, why it got launched more or less end of '24, that business in the U.S. is very much a tender-based business. And these tenders are typically 3-plus years. That means only every year, 1/3, 1/4 of the market is addressable for us. So we're still rolling nicely into that business that will drive growth for still quite some time.

I want to hit on margins quickly. So you previously discussed there's a path to pull forward the 31% margin target. Now we're thinking about flat to maybe slightly down this year. Obviously, some FX headwinds in there. But how should we think about the confidence in the 31% framework?

In fairness, there's a couple of headwinds, right? First of all, we did an acquisition where we clearly said it's dilutive, where it's 100 bps, right? The United States decided to implement some tariffs, right, which is also quite some headwinds. And currency wasn't helpful either despite that fact we were growing margins, right, last year; and despite that fact, we are probably keeping it somewhat flattish with what we said for this year, 29.5% on a constant exchange rate, which the actual rate is probably 29-plus percent in all fairness.

So I would say we still continue to expand margins. We still have 40 efficiency steps going forward to helping us to expand margin as well. And on top of that, of course, overall, the menu direction is being very helpful. It's no surprise to you to anybody else that Sample prep at QIAGEN has probably a higher gross margin than most other products. So if Sample prep continues what it is doing right now, being growing quite nicely, the mix will be helpful.

We always have been quite open that QIAstat is an important product in terms of margin expansion because the utilization of production is an important topic in that environment. So again, as we said by yourself, we do believe that it's a good product which is going to grow as well. Yes, I don't see any reason that margin shouldn't improve. Again, I hope that you're not increasing tariffs every second month. But despite that factors, which we cannot control on the efficiency side, we are in the middle of stepping up on changing our ERP system, bringing 2 systems to 1 system. There are a lot of detailed projects behind that. There's clearly updates on that coming up.

Yes, a little bit -- just under a minute left. Maybe the door is open to ask about the strategic process, and we talked on the CEO timing. Maybe just talk about where the Board says that you announced to the world you hire bankers. So what...

Yes. As we said, as you know, a couple of -- probably a few weeks ago, we announced that we engaged 2 bankers to help us and help the Board to review all the different options, which we have. Clearly, also a reaction on all the rumors being around since the announcement of [ Thierry ] and QIAGEN taking part. Nevertheless, I do think there's also an important event which we described before, which was important for shareholders, which was the Capital Market Day. It is probably important for a lot of different parties. So let's see how that plays out and then we take it from there.

Okay. I'll leave it at that. Thanks.

Thank you, Tycho. Thanks for having us.

Thanks for joining us for our next session. My name is Mike Ryskin. I'm on the Bank of America Life Science Tools and Diagnostics team, and we're excited to be hosting Qiagen. We're joined by Roland Sackers, Chief Financial Officer; and Domenica Martorana. Format will be a fireside chat Q&A as usual. Raise your hand if you've got any questions. Happy to let you jump in.

Roland, had some updates yesterday from you in terms of the Board meeting updates, things like that. Anything specific you want to call out from there? We saw some changes to the Board, a little bit of an update on CEO timing. Just maybe you could talk through some of the key takes from that.

Yes, sure. And first of all, thanks for having us. It's always a pleasure to be here. It's a long trip, but it's, for sure, worthwhile the trip. And again, thanks for having us. 2 days fully booked. But I do think what is important, and you will mention it, that yesterday, we released the proxy for the upcoming AGM. I do think it has a couple of exciting news.

And I think let's start with getting certain things out of our way. Probably very important is we are asking for approval of more share buybacks. As you know, Qiagen has this, I would say, setting that we do, 2 different kinds of share buybacks. One is open market share buybacks or on the market. Here, we asked an approval of up to 10% of our total capital. And the second one is, what we call in Europe, synthetic share buyback, which is -- also, here, we are asking for approval of another $200 million of synthetic share buyback.

Again, it's for approval. Typically, its approval holds for 12 to 18 months, and then it's up to the Board to execute on them whenever they believe it's a good time for them. But nevertheless, if you see that in combination with the $500 million share buyback, which we did already January this year and also what we did over the last 2 years, you can see that there's a clear commitment also here again on increasing shareholder returns.

Second topic was that we continue to, call it in brackets, refresh our Supervisory Board. We have just seen that a new Board member was actually on stage here before, which is Bob, CFO of West Pharma, which I think is a great addition, given his track record, his industry experience. So we are very much looking forward that he gets elected on the AGM in June. And at the same time, our -- one of our founders, Metin Colpan, who was, by definition, of course, for many years on our Supervisory Board, is stepping down and becomes a non-voting Honorary Chairman of the Board. So I think -- which is again, on one side, a great recognition what he did over the last 40 years for Qiagen at the end of the day.

Last, but not least, you were also referring to the actual status of the CEO search. What we also said is that Thierry stands for reelection on the upcoming Board AGM to be a Managing Director for Qiagen until we are announcing incoming CEO. I think what we are believing right now it's an H2 event.

And I think what you can read into that is that Qiagen is still looking into different directions. You still know that there is an ongoing strategic review. And therefore, again, I think it's also quite clear that the Board, but also any potential candidates want to see how that works out. At the same time, I can guarantee you we don't have any shortage of candidates. So we do believe that is a good timing for the company.

Okay. Okay. All right. And then you mentioned the share buyback. There is also a dividend increase, too, right?

You're absolutely right. I shouldn't have forgotten that. We are also increasing our dividend by 40% to $0.35 EPS, which again shows also our commitment to shareholder returns. For us, it's an important signal that we also feel very confident about cash generation in the company, and we are committed to our net debt-to-EBITDA goal, which we'll virtually launch more or less earlier this year.

Okay. Okay. All right. Maybe let's talk about the other update from the last couple of weeks. The 1Q results, you guys gave a flash, and then the full result last week, had to update the full year guide. There are a couple of different moving pieces. I think the most notable one was QuantiFERON tied to immigration. Maybe just talk through how the quarter played out relative to your expectations, where the surprise came from, just sort of how you're incorporating that into your forward outlook.

Yes. First and foremost, that hasn't changed for the year. As you know, we are focusing on 5 pillars of growth. 4 of the 5 pillars of growth, we just confirmed, full stop. Within the fifth pillar, which is QuantiFERON, we clearly had to identify that the immigration piece of that business is going in a different direction than we initially thought.

Just putting things in perspective, QuantiFERON is around about a $500 million business for us. 90% of that business, no change at all. The 10% immigration piece of $50 million is something what we had to revisit and particularly in U.S. and somewhat in the Middle East. So just to break that $50 million down even further, $15 million is in Europe, 1-5, no change at all.

We believe that is an ongoing business for us. We haven't seen any change. $30 million is more or less the U.S. part. We took that out fully. Given the political landscape right now, we don't even see any opportunity that it comes back in any reasonable timeframe. Of course, it's going to be in the base as of Q1 next year, but we have to go through that period. And there's another $5 million around about, which is related to the Middle East business, which we have in QuantiFERON, which again is clearly a business, which we believe at least temporary with the ongoing war, is somewhat impacted. Nevertheless, we took it out 100%.

I would argue, at some point in time, it comes back because there will be still construction and other workers have to fly into these countries. And -- but again, it's hard to say when that is going to happen. And if we have to reset the guide, we rather than turn every corner and every stone and see that. So Q1, everything was overall as we expected it. We were, at the end of the day, $10 million down, $8 million was what I just mentioned.

Okay. And the $30 million change in immigration outlook, QuantiFERON-tied immigration in the U.S., is that tied to any new specific policies? Is that just sort of an implementation change? Why so sudden, why so drastic now versus fourth quarter, third quarter, second quarter last year? I mean, assuming this is tied to the administration, why now?

It's a very fair question, and you can hopefully believe that we beat ourselves over the last couple of weeks quite significantly, should we have seen it earlier. But I think the matter of the fact is we as well as our customers have not seen that more or less before Q1 happened. Have in mind, the immigration-based testing is not done in any kind of specialized dedicated lab environment. It is done in the very normal lab facilities, whatever you think of, Quest, Labcorp, ARUP, you name them.

And so it is happening under a very general setting. And we had very normal order incoming actually all the way into January. So in January, things started to change. When we went to our customers and asked, okay, guys, what's going on, and together with our customers, we looked into the different labs and then we figured out certain regions having no impact and certain regions have a different impact. So again, if you just looked that in Texas, significantly larger impacted. Middle East and some other areas not impacted at all. And then you started again to look at that.

In hindsight, you can clearly argue, as you know, certain immigration topics changed legislation-wise in June last year, but didn't have any larger impact. A big step-up in terms of countries was actually mid of January. I'm not sure if that made an impact, but sometimes things slip over.

But I think what we also have learned is that there's a lot of, what you call it, libertarian organizations doing healthcare for also illegals. And that is probably also where we have to realize now that they're running in funding situation and others, so things adding up. We took here probably a very cautious view, but it's just saying it's hard to identify for us what exactly stays and whatnot. Take out 100% and if it gets better, fine.

And what about -- you mentioned the 90% that's not immigration, the other $450 million. What's the underlying assumption for growth rate there in 2026 and beyond?

We haven't reset the bar yet right now. So again, we believe right now that -- as you know overall, we had this kind of 5%, 6% growth rate. I think that is probably for the remaining part, still a reasonable assumption. What we still have to figure out how quickly is now the resetting of the inventory level is going to happen. I would assume that it probably takes at least the second quarter, and then it should improve somewhat in the second quarter -- sorry, in the second half of the year, particularly in Q4.

And is it too early to say for 2027 and beyond, especially that U.S. immigration bit, is there an expectation that comes back at some point? Is it just sort of easier to just not even think about it and pretend it's not there? Sort of how are you approaching it?

So one thing we shouldn't forget, and again, it got confirmed today on a different location, everybody is, I think, agreeing that the overall TB testing market is growing. We say 4% to 5%. Others say 5% to 6%. I think our 4% to 5% is still on the conservative side. Still assuming, which I think nobody disputes either, that that skin test market is still 60% of the total market. I think it's fair to believe that we will grow at least that market growth and hopefully better than that with this ongoing penetration.

Okay. I think you're alluding to an Analyst Day that happened earlier today from one of the other...

Competition with [ UMN ].

Yes, yes. From one of the other major diagnostic vendors. Just anything you kind of took from that in terms of updates on their test and their offering?

Again, not much surprise for us, but it looks like probably for some shareholders because share price reacted positively, I think there's a couple of news which further of all, I think, got confirmed what was rumored before that they are missing a couple of parameters in particular, CD4 and CD8, which are very critical for selected groups of patients, again, particularly if you're looking at immunocompromised patients on. So I'm quite sure that that will have an impact.

Second, I think the workflow expectations were probably somewhat overestimated. It looks like that there's still quite manual steps, didn't even articulate it, from my knowledge, to an extent that it was clear to the market. No news on U.S. launch, at least what we have seen so far. So I would say, again, for us, no surprise. For probably some shareholders, some incremental news.

Okay. All right. So that's QuantiFERON. We handled that. Let's talk about the other component of the full year guide revision was sort of just the broader life science market and expectations for that. Like you said, didn't really factor in a big way for 1Q because it really did seem to be immigration-specific, but you are taking down your assumptions for the rest of the year. What drove that? How did that play out in the quarter? And why do you think the new outlook is more representative?

Just to be very clear, we actually haven't changed too much. The one thing what we changed is particular QuantiFERON immigration-based testing, the $35 million. The second area which we have tested was rather OEM-related. These are literally a handful of customers who do typically high-7-digit deals with. Here, we just took a more conservative view. Even if we sometimes have orders on hand, but the political landscape is sometimes very difficult to read, right?

So for example, we have larger contracts with U.S. governmental institutes, where typically, we have an ongoing business. But sometimes, given particularly that environment, you're not sure if they are able to execute on that. Now when we had to revise our guidance for QuantiFERON, in brackets, anyway, we turned every stone and see is there any potential risk just to make sure that things never happen, at least not -- likely not happening again. So we identified more or less 2 of this kind of isolated topics.

The overall life science business, as demonstrated with our sample prep business, I think it's moving in the right direction. We anyway always had a quite stable life science business. You remember that sample prep in general last year was good. We were always cautious on the instrumentation side. We do believe it's going to improve somewhat, but that is not the driver for our acceleration this year. The driver for our acceleration from H1 to H2 is, first of all, there's 200 basis points of headwind from discontinuation of business last year, which was NeuMoDx and DIALUNOX as of June 30 last year. That will stop by definition mid of this year. So 200 basis point improvement of that.

Another 200 basis points comes particularly out of new product launches, which is, in our case, particular sample prep. You know about QIAsprint, our new high-throughput machine. You know about QIAsymphony, which is also on the market, so there's no launch risk. But of course, it has to accelerate over time. So I would say this incremental 200 bps or $20 million revenues is not unlikely, given the $700 million base we're having.

And last but not least, we also do believe that Parse, our recent acquisition in the single-cell business, should accelerate and probably do also better than the expecting $40 million, which we put into our numbers earlier this year. So I would say there's literally no larger impact from a life science acceleration in our numbers. Of course, we like to see that, don't get me wrong. And I think there's also early indication also on the instrumentation side, but I wouldn't call it victory yet.

Okay. Yes. I mean you touched on Parse. Let's go there. It looks like that was a little bit better than expected in the first quarter, at least relative to your $40 million assumption for the full year. It's tough to draw any conclusions from 1Q, but is there anything specifically that you could call out that drew that strength?

I think just the technology, the single-cell technology, that is very much requested. And also, together with the scalability of that part of the business and just the proof points that we have on large datasets, that's just something that makes us very confident to overachieve the about $40 million that we set for 2026.

And here also, just the synergies that we see also with our bioinformatics business is an important piece as well. So it's not just about Sample tech and Parse being part of the Sample tech business, but also our bioinformatics business that we have.

One of the benefits we have in clear with our Parse technology is that is instrument-free. So you can use it just by using the product itself, which in that environment is not a bad situation. The same thing where we're seeing right now, we're doing actually quite well in front of pharma customers.

I do think Qiagen is, of course, given our global presence, a good acceleration factor for the overall Parse business. So I think the combination of that, plus what you just said, the integration of our -- with our bioinformatics franchise, which will take a bit more time, should be helpful to drive that business going forward.

So you're still assuming $40 million for the year. You just kind of see... That's more upside than downside. Okay. Going back to what you were talking about earlier, Roland, in terms of the new product launches in Sample tech, that's kind of factored into the guide as part of the second half ramp. What are your -- anything you can give in terms of your assumptions for that contribution, confidence in that coming through?

The good thing on instrumentation business, you typically have a pipeline. And I would say the pipeline so far is building quite nicely. So I would say we feel this, particularly with QIAsprint, which is our new high-throughput platform, I think the pipeline build goes quite well, and we should see the first numbers already in the second quarter, but as you said correctly, much more important in the third and fourth quarter.

We also expect, given that it's a high-throughput platform, that the consumable pull-through starts quite nicely. Majority in the beginning will be in life science. So I think also there will be, as always, reagent rental business, but there will be clearly at least 50% of straight sales, which should be helpful for us. So again, I think that is something where we have good confidence.

symphony, same thing. Here, we are, of course, working with particular customers like the Guardants or Nateras or whatever, who are already existing customers, to roll that out because it has significant advantage for them as well. So again, on the sample prep side, again, at least, you know what, now we have the organic growth rate of 3%. If we're able to keep that and grow that over time, that's a nice thing for us.

Okay. Okay. And you talked about -- earlier in the session, you talked about how outside of QuantiFERON, if you think about the growth pillars, the other 4 were on track. Your assumptions for the other 4 for the rest of the year have not changed. So maybe let's talk a little bit about QIAstat, QIAcuity, QDI, sort of how the quarter played out.

There's always some doing better, some are doing okay. I think outstanding, as we talked about, and we're going to repeat it with sample prep, clearly a healthy start to the year. I think the same is true for QIAcuity, double-digit consumable growth rate, double-digit instrumentation growth rate.

As you know, we have a significant project in enhancing our portfolio in terms of assays and panels. In the last 2 years, we launched every year around about 100 different assays, panels on the machine. This year, we said publicly, it will be several hundreds. So we do believe that end of this year, probably in the second half of the year, we have probably the broadest menu available. We also have GeneGlobe, where people can define their own assays. We produce them and ship them to them, which is a great advantage. Customer loves that.

QIAstat, I would say, good start into the year, given that respiratory last year in H1 was a huge business. We also told you ahead that also Q2 will be not the easiest quarter for us because of the respiratory headwind. Placement numbers in Q1 were good. Quite sure that Q2 will be also very healthy, [ gust for ] double-digit growth rate, many guided double-digit growth rate. So I think we are on track to having our $160 million of revenues here as well. QDI, also a solid start, high single digit. It's okay.

Okay. And outside of the growth pillars, PCR, genomics, CDx, that was a little bit more mixed, a little bit spotty in the quarter. Is that more of an end market dynamic, given some of the softness you're seeing in A&G? Is that specific customer issues?

It's somewhat expected -- in all fairness, it's probably a bit weaker than we thought. We do believe -- it was double-digit negative. We believe it should be probably more like mid- to high-single negative. Of course, have in mind that also in that area, we stopped [ exogenous ] and some other products. So there is an impact of that, which has to wash out.

At the same time, it's probably also somewhat of a conversion to digital PCR. It's the reason why we expect some negative numbers into that. So I think we will have a bit more focus on that, stabilizing it in the area I indicated, and that should be helpful as well.

Okay. Are you -- from an end market perspective, are you seeing any stability in A&G? Have things sort of resettled at a lower level? And then we'll talk about biotech and pharma as well.

I would think things are moving in the right direction. I think it's still a bit on the level of, let's have some more confidence. But again, you know that we last year -- also last year, we had a quite solid consumable business overall. I don't think that has changed. I think what has changed now over the last couple of weeks is that we get more request for proposal for instruments. Again, we're not calling it victory yet, but at least people are trying to familiarize themselves what's going on.

Okay. Is it -- you mentioned reagent rental. Is that coming up more and more where people are a little bit more...

On the diagnostic side, I think it's typically part of that, on the life science side sometimes, but it's not a big tool.

Okay. Okay. And in terms of specifically U.S. A&G versus Europe or potentially China, anything to call out by region?

China is selling. As you know, for us, it's like a 4% of share. We have seen some improvement, still negative. I hope or we hope that end of this year, we are only slightly negative, maybe flattish. So it's improving, but it's not in positive territory.

Okay. Let's talk about operating margins and leverage. You -- despite some of the top line weakness, you're still able to deliver some impressive numbers on the OpEx side of things. Just walk us through the bridge there. What's allowing you to do that despite the...

Just to repeat what you just said, we reconfirmed the operating income number for this year, 29.5% at constant exchange rates. So with actual rates, it's probably 29-plus percent, which is despite the negative impact we have from the Parse acquisition because we clearly said we are doubling down on R&D investments, so it's 100 basis points dilutive for the year. And so I think -- nevertheless, we still see gross margin stepping up somewhat, not only this year, but also particularly also next year, mix getting more favorable.

A big driver for us is still the QIAstat utilization ratio, because as you know, this whole production environment was built during COVID. So there's room for us to go into that and get into better standard costing mix, as I said, in general. But we also have 40 initiatives, we call it, of course, QIAefficiency programs and which are ongoing, and there is certain larger programs in -- like the rollout of our new ERP system. We are going to SAP HANA, which we do in steps. But of course, we are moving on here.

It's overall digitization of the company. We have now in the meantime 60% of our orders coming in a digital way, which again, clearly takes quite a significant number of cost out of the system. So there's a lot of detailed projects, which we track quite well. And as you know, they helped us to improve margins over the last 2 years. I don't see any reason why that should change over the next few years. We have, I think, a commitment out by 31% by '28. We clearly said before that we are able to increase that target. Now we will wait for the new CEO to launch it, but I don't think the underlying tonality is not going to change.

Okay. Yes, we'll talk about the mid-term targets in a bit, but on the '26 margins, just to be clear, did you -- are you taking any incremental cost actions post-1Q to sort of reaffirm those numbers? Or is that just still...

I would say we still have cost action, but the plan of underlying -- long-term plan.

Okay. Okay. So on that mid-term framework, you previously outlined so that 7% core sales CAGR, the 31% operating margin, which seems to be coming on the higher end of that, $2 billion of growth pillar revenue. You've had some tweaks here and there, but how comfortable are you with those mid-term targets?

I think we're comfortable with the $2 billion. I think it's fair enough to say that the mix will change, but we're probably a bit short on QuantiFERON, most likely, but that we will overshoot on sample prep and probably some others, the QIAcuity, and for sure, QIAstat. So again, the mix will change. The $2 billion should probably stay.

We are done already with the share buyback, which was $1 billion. We will clearly overshoot that, but we announced not only this year, but also more or less -- hopefully, the shareholders are going to approve in June. The margin committed 6%, 7%, we'll see a bit, right? It might be -- 7% might be a stretch. Let's see how we go.

Okay. And you talked about share buybacks at the beginning with the AGM, just kind of touched on now. Can you talk about new capital deployment priorities going forward? Just between the dividend increase and the share buybacks, is there room left for M&A? Sort of how do you prioritize that?

I think our commitment to all 3 areas has not changed, and I wouldn't put any kind of either/or into that. So we -- first and foremost, we clearly want to invest in the organic growth of the company because it still has the biggest return opportunities for us, and therefore, for all our stakeholders. Second is we like to do bolt-on acquisitions, like we did with Parse. I think it was a great fit to the company. We don't need something transformational, but if something fits to our portfolio and accelerating the portfolio growth, happy to do so.

The likelihood, of course, that these deals happen quite regular is somewhat remote. So while we're doing quite busy, so I think there's enough opportunity, given also the underlying cash flow and the leverage we're having that we can continue in doing share buybacks, increasing dividends over time as well. So I don't think it's an either/or. It's really and.

Okay. And on the flip side of that, you've not been shy about divesting or discontinuing or one way or another trimming things that either are noncore or underperforming. Do you feel like the portfolio is pretty well cleaned up at this point? Or is there more room to fine-tune?

I would say so far, we feel quite comfortable. Again, let's see if -- I don't think there's any larger strategies change, if there's a new leadership team or so, but you never know. So I would say that's something that we have to demonstrate. But in general, the growth drivers deliver right now somewhere between 6% and 7% growth rate. I don't think that is questioning anything. And I do think the leverage probably right now comes out of operational efficiency, and that should give us also enough room to grow margins going forward.

Okay. And on the -- going back to the topic of the CEO change, could you give us any insight in terms of the criteria the Board is using or sort of what are the priorities? Is -- you've outlined certain strategic initiatives and moves. Is the goal to find a CEO that fits within that framework? Or is there a view where you might have a new CEO and some of that framework could change?

I probably think the way the searches I've done in this world is that I would not expect any larger surprises, at least for the Board, because typically, as you know, these candidates go in the meantime through quite a dedicated search process, have to present their cases and so on. So I think everybody knows quite well, from both perspectives, what to expect and that there is no larger surprise, right?

At the same time, I do think what the Board expectation is. Yes, we'd probably call it looking for somebody, in brackets, who has seen the movie. So somebody who worked in life science, who worked on the clinical side as well, some -- because we clearly have a business in both parts of the industry. We clearly would love to have somebody who has experience with Europe and the U.S. because we have an operational setup, which is actually very global as well. So there is a good set of candidates out there. And so I'm quite comfortable that we have the right candidates.

Okay. Last couple of minutes left. Any questions from the audience? If not, Roland, maybe our standard closing question, or remark, sort of what do you think is most underappreciated? What are some of the bigger debate points you're hearing? Anything you want to clarify to investors or make sure people take with them as they walk away?

I'm not sure there's something underappreciated. I think there's a lot of things overappreciated, which was the fear about QuantiFERON, and the world is falling apart. And so I really hope that with some of the news coming out probably today and then hopefully get more interpretation over the next couple of days, and hopefully, the products finally make it to the money -- to the market that people will figure out that there is still the leader in QuantiFERON in TB market and that's Qiagen and that we continue to grow with QuantiFERON, but also in particular outside QuantiFERON.

That is all what we want to demonstrate because nobody questioned, I think, that we delivered quite, I would say, a series of 26 quarters in a row in terms of revenue and EPS performance. That is what we want to do going forward as well.

Okay. All right. Well, on that note, we'll wrap it up there. Thank you so much. Thanks, everyone.

Thank you.

Thank you.

Welcome to our spotlight session. Today, it's all about QuantiFERON. And in the next hour, you will learn more about our strategic priorities and the latest developments. But before we start, let's have a closer look into the legal disclaimer.

As with any investor event, this presentation includes a safe harbor statement. You're likely familiar with this from our other presentations. So I won't read it in full. However, please remember that we will be making forward-looking statements. Actual results may differ materially from those projected, and the factors driving those are detailed in our most recent Form 20-F filed with the Securities and Exchange Commission. A copy is also available on our website.

Today, I'm not alone in the studio, and I would like to welcome our CEO, Thierry Bernard. Hello, Thierry, and good to have you here. Over to you.

Thank you, Domenica, and good morning, good afternoon, good evening to all of you. Thanks again. for your attention and interest in Qiagen. A year ago, and I hope and I think that most of you attended that event a year ago, we organized an Investor Relation deep dive session on quantified. And we wanted to leave you with 3 main messages.

One, tuberculosis is still the main infectious diseases killer in the world. Remember, tuberculosis continues to kill more than HIV and malaria every year, 1.6 million of people will die every year of tuberculosis. But the reservoir of active tuberculosis latent tuberculosis is even a greater health care challenge. 2 billion people in the world are estimated to be impacted by latent tubercolosis, this is an incredible number.

Second, Qiagen is the undisputed leader for more than 20 years now for latent tubercolosis is testing. But despite being a leader, we have never been complacent or arrogant and we have continuously invested into the development of our solution. First, if you remember, back in 2016, the front-end automation and the unique partnership with a leading company in immunodiagnostic DiaSorin.

Second, the continuous improvement of our test itself to keep and its chemistry, bringing the only combination, I repeat only combination on the market of CD4 and CD8, which is so critical to be able to manage specific population of patients, like, for example, immunocompromised patient. Think about HIV patients hepatitis patient. QuantiFERON latent TB testing is by far the most sensitive test on the market.

Third, improvement after the automation of the back end of the test with DiaSorin, the automation of the front end of the test with partners like Tecan, Hamilton to leading companies again.

The third message we wanted to leave you with a year ago was the market potential is still significant, especially the market conversion of skin test and antiquated technology. And we told you -- but the best -- or the best estimation today are that we still have around 50 million, 5-0 millions of test skin test in the world. ready to be converted to a more modern approach like Qiagen QuantiFERON. Just in the U.S. alone, it's 15 million to 16 million of skin test to be converted. But we don't want to stand still.

Today, we are coming to you to announce that 3 leading companies are reserve strengthening or creating new collaborations to bring an even better set of solutions to our customers. First, DiaSorin, our partners for quasi 10 years now.

Second, a leading company in full engineering and automation in [ Peco ] and we will have their CEO, Ricardo reserves today.

Third, Qiagen, of course, continuously investing into our solution. First, new innovation, and you heard about it at least in Europe, is an unprecedented improvement of the efficiency of our current test. Turnaround time is of use. We call it clear to already available for some months in Europe now available as well in the U.S. Second, innovation today, the first and probably only end-to-end automation, sample in result out automation for Quantify.

For the first time, 2 companies together with DiaSorin are bringing the first full automation workflow where a technician will just need to put a tube into the system and wait for the result. And third, a unique and clearly only possible for Qiagen because of 20 years of test, a unique AI investment to help doctors determining tomorrow, who in the whole population of latent TB patient has the highest score to move to active TB. This is tremendously exciting. This is innovation at its best. But even so, it is also confirming that Qiagen doesn't take our leadership with complacency.

Thank you, Thierry. Innovation clearly doesn't stop here. And with that, let me hand over to [ Nadia Albrecht ], who is going to tell more about our unique QuantiFERON ecosystem.

Hello, everybody. It's great to see you at this QuantiFERON Spotlight event. WHO has announced that by 2035, they would like to eliminate tuberculosis. You can only eliminate tower loses by working on your active TB cases and treat your patients, but you should also look for the reservoir. And this reservoir is latent TB or TB infection. 25% of the world population are about 2 billion people are infected with latent TB. Qiagen estimates the global latent TB testing market at approximately 75 million tests annually, growing about 4% to 5% per year.

Only about 40% of this market has been converted from traditional skin test to modern blood-based interferon gamma release assays or IGRAs. Patients that usually get tested are immunocompromised, health care professionals people that live and close relationship with an active TB patients, but also other groups. All of this together makes a market potential of 1.6 billion in 2026. During our deep dive of QuantiFERON of last year, we told you that we would continue to invest in our QuantiFERON portfolio. And this is indeed what we have done. From the beginning of the acquisition of Cellestis, Qiagen has nonstop invested in making our QuantiFERON assay better, more specific, more automated and more reliable.

When we launched our fourth generation, we added a patented CD4, CD8 antigen technology. And this has allowed us to have a more reliable assay for critical ill patients like immunocompromised and HIV. The magic happens in the tubes, but we never stopped looking and how we can further improve the test. Today, we are proud to present our next step in workflow enhancement and the creation of a QuantiFERON ecosystem for improved automation and patient management.

The first improvement is the launch of a new LIAISON chemistry together with our partner, DiaSorin. The new chemistry is designed to improve speeds, throughputs and workflow efficiency by enabling labs to test up to 75% more patients per hour and achieving a 25% faster turnaround time compared to the previous version. It was launched in November 2025 in Europe and recently launched in the U.S. after receiving the U.S. Food and Drug Administration approval in February 2026.

The feedback of our clients are very positive, and we are on track in our conversion plan between the old and the new chemistry. Latent TB testing is moving towards higher volume, more automated workflow as the market increasingly shifts from traditional skin test to modern era based detection. Qiagen has been investing in automation for several years, partnering with companies such as Tecan and Hamilton, to streamline pre-analytical steps and with the actin to automate the detection on the LIAISON platform.

But we felt as the market leader that we had to go a step further and aim for a full automation, enabling labs to scale with growing demand. This is why Qiagen, leader in globe-based latent TB testing and Peco, a leader in lab automation, and DiaSorin, leader in high medical value testing have started the development of the first full automated block-based IGRA testing platform that we plan to launch by the end of 2027.

The lab technician will only need to load the samples and all the other steps in the process will be done automatically. And the right sequence and at the right time. This is the first and only blood-based IGRA test for higher volume testing that will be fully automated.

[Presentation]

With this partnership, we are leading, again, the next-generation blood-based IGRA testing, and we will have an automated proposal linked to the volume needs of our clients. 20 years of experience, 4 generation of test, multiple endorsements and more than 2,700 publications. We are the only company that has this experience. Based on this, we are creating an AI-enabled risk certification to -- for TB progression with the goal of supporting stratification of patients at a higher risk of progression to active TB disease.

With this tool, we are creating a real sample to insight QuantiFERON ecosystem. This tool will use the values of our 4 unique QuantiFERON tubes, along with other parameters to deliver a more complete view of the immune response to TB. The tool is built on one of the largest longitudinal TB clinical data sets, comprising about 13 million de-identified patient records collected over the last 10 years. And is intended to support health care professionals and making more informed decision, improving patient counseling and supporting enhanced patient care. At Qiagen, we nonstop continue to invest into QuantiFERON as we grow with our clients and we answer the needs of this growing business.

Thank you, Nadia. And Nadia will also be here with us in the studio for the Q&A. The topics, detection, automation and AI-enabled risk stratification Cherry, let's focus for now on automation. And for that, I would like to welcome the CEO of Inpeco, Riccardo Triunfo.

Yes, indeed, we have Ricardo with us. It's an honor, Riccardo to have you with us this morning. Let me start with the first question. You're a leading company in engineering and live automation explain to us why is end-to-end automation so critical for customers those days.

So first of all, Thierry and thanks for this invitation. I think we are all proud to announce this joint impactful innovation. So to answer your question, let me start from our vision. So we, as a company, we believe in a world where medical errors are eliminated through lab automation, software and data traceability. We all know today, labs are facing what is called the perfect storm, chronic shortage of skilled staff and a massive increase in testing volumes. And that end-to-end automation is in our view, the best way to solve this.

By removing manual touch points, we reduced the potential for errors and ensure the full traceability from the moment a sample arrives until the final result. This allow labs to scale their operations efficiently while guarantee the highest level of clinical integrity.

That's very good. And Riccardo, if I may, I have a second question for you. like us, like Qiagen, you work every day with the biggest labs in the world, the quest, the [ LabCore Serba ] in the world. Why do you think a purpose built automation, full automation for QuantiFERON would make sense for those kinds of customers.

Yes. Thanks, Thierry. I mean it makes a lot of sense because laboratory today serve a massive spectrum of needs from small specialized labs to large centralized facilities that you mentioned. With an increased sample volume. The challenge is how do they scale operations and reduce manual steps simultaneously. This is exactly where I see our partnership makes a difference. Inpeco is not just providing a track to Qiagen. We are integrating a fully automated full automation for the entire diagnostic workflow through our flagship automation, the [ Flex Lab ] with new dedicated modules and software.

So by combining Qiagen leading detection capabilities that we have seen with our DNA in automation, we are creating a truly integrated and fully automated solution for QuantiFERON latent TB testing -- throughput and reduce ends of time. And let me say, more importantly, create a super standardized, repeatable process that brings long-term value to the health care system and the labs across the globe.

That's really exciting. I think, Domenica, that you had another question for Riccardo as well.

So one last question from my end, Riccardo. From an investor's perspective, and I think they will be very interested about that. But when do you think the first systems will be up and running at our customers?

No, it's our commitment to move with the greatest momentum to bring this next-generation system to the market. Our ambition is to have the solution fully up and running in laboratories in late 2027. And now we are in a phase where obviously we are also understanding if this can be anticipated. But the forecast is late to 2027. Thanks for asking.

The good thing, Domenica, to leverage a bit what Ricardo just said, is that we have already under CDA presented together with Ricardo sometimes separately. The solution to some key customers. And what I can testify today is that the reception and also input from those customers have been -- hello there -- sorry.

So as you've seen, we now also are joined by Nadia in the studio. Welcome back.

Hello, Domenica.

Hello. So we're ready now for the Q&A and taking your questions for the Thierry and Nadia from the studio, and we also have some more speakers for you today. Welcome back Riccardo. And we also have, as a speaker, Nitin Sood, you know him from our last events, Head of Product portfolio and innovation. And we also have for you ready to take your questions, [ Parampal ], who is the Head of R&D applications for QuantiFERON

Before we start, just as a quick reminder, if you haven't done so, please type in your questions into the Q&A box into the web portal, and we're very happy to take them. And I think we're ready for the first question, right? So let's start with the first one. Are there any competitors currently offering end-to-end track-based automation for latent TB testing and how differentiated is QuantiFERON's position in that area.

Well, the answer is very simple, Domenica, it's no. First of all, even as of today, with the current workflow, Tecan or Hamilton, QuantiFERON and DiaSorin, there is no comparable automation. And tomorrow, this will be unique and really specific to QuantiFERON. So the answer is clearly no. It's at the moment, unprecedented.

So the next one, do you expect -- sorry, I jumped, give me a second. There's lots of questions coming in -- that's why it's jumping. So apologies for that. Do you expect an impact of AI-enabled decision support on testing volumes or market expansion?

Well, I'm going to ask Nitin to take that question because, obviously, you understand that we are taking a bit here. It's a very well-considered bet. It's a fantastic evolution because the holy grail in the fast -- in the fight against TB will be that ability to detect or to predict predictive biology, who in the population of latent TB has the most risk to go to active TB. So what do you think, Nitin?

Yes. I mean, I think, first of all, I just want to emphasize the fact that only we get business intelligence into the test is risk-based progression score because only we have access to these 30 million patients than a longitudinal data.

And again, I just want to remind everyone that most people who have latent TB don't have active symptoms and may not follow through with their treatment. And therefore, providing this intelligence to the patient or to the physician will increase compliance to treatment. And that is a big differentiator, and we absolutely hope that will allow us to expand our leadership position in the latent TB franchise.

So the next one is on the partnership with Inpeco. The development of end-to-end automation solution, is it purpose-built for QuantiFERON?

It is, but I would like to invite also Riccardo to give also his vision here.

Yes. Thanks for this one, Thierry. So while our history is completely rooted in an open automation, this project has been ideated and will be developed with and for Qiagen specific. So we are developing a new ally quarter, which is specific to the testing, as you have seen in the video and an intelligent incubator that have been designed ground up specifically for the QuantiFERON test.

So this level of specialization, which is incorporating Qiagen specific configuration and workflow design is exactly what allows us to guarantee the high level of throughput and the -- reduction, which is also defining our mission. So that's why we are prioritizing the integrity of the specific test will ensure the highest standard of patient care. And that's why this test is specific, this automation and workflow is specific for Qiagen.

Yes. So the next one is on partnerships, right? So what drove the decision to partner with Inpeco versus QIAGEN's prior automation partners such as Tecan Hamilton. What is the value? And the next one is on AI. Let's keep it for now on Tecan Hamilton.

On Inpeco, I think it was a choice that became very clear to us when we decided not to think about automation in terms of adding some different instruments, but thinking from scratch and say, why don't we build something purposely for our test. And therefore, Inpeco, a company that we have been respecting for so many years, and we knew that, guess what, they were present, where we are present. They are present in our biggest customers. We see them every day. It was a natural partner.

Let's now move to the AI question. So the value of AI-enabled risk ratification and which segments of the testing market would this be most relevant for.

I think first, we should probably give a bit of science with [ Par and pole ] on what we are trying to achieve. And then I will ask Nadia to take that question on specifically the patient population that we are targeting. Paranpal?

Thank you, Thierry, and hello, everyone. I want to say a few things. I'm so excited to say this, Qiagen has acquired 13 million unique de-identified patient sets. And Qiagen is the only company who has this breadth of testing, and these data span from 2017 numbers. So it's almost a decade worth of data. And the key here is the long issue -- now data. That means that the patient has to be tracked or tying and we need to have full history of multiple QuantiFERON tests and all other patient parameters, which go with the testing to diagnose the latent TV to active TB.

And the value of CD4 and CD8 is so unique to Qiagen because it gives the comprehensive view of the immune response. These patients are already sick and they could be immunocompromised and this is what advantage QuantiFERON test brings to the table. So that being said, these data sets are spanning from all geographic distribution of U.S. It has pediatric to geriatric population, which is so important for the TB disease, and this will allow us to have a full comprehensive view of immune response for patients at an individual level. We already know that these risk factors are determined at a CDC and WHO level at a population level. But the key is what about the patient level, and that's the beauty of this risk score. Risk stratification, a tool which we are bringing to the table.

Thank you, Paranpal. Nadia, can you say a word about what kind of patient segments would be even more interested?

Yes. So thank you, Thierry. For the patient segments, according to the guidelines in the U.S., every latent TB patient needs to be treated. But as Nitin already said, if you're not sick yourself and you need to start a treatment, sometimes it's difficult to convince the patient to be treated. So this is why we hope this tool can help the clinician to show to their patients, the added value of getting a treatment and why it should be done. So in principle, it is going to be done for all patients that a clinician sees. We know that some people are very at risk. If you take biologics and if you're immunocompromised, these are very high-risk patients. but it's really to convince a patient, please follow your treatment and finish your treatment and don't stop it because this is surely not good.

So we have a couple more on AI. Maybe we'll stick to that for a moment. institutional organizations like WHO migrations officers and so on, we'll probably be very interested by the AI tool that we already started to discuss with them and what's the input on that?

I would say that Qiagen is a, first and foremost, a fact-based company. So we try to avoid making claims as long as we are not clearly sure that we are saying -- what we are seeing, what we are bringing to the market is proven. And so before having those organization, WHO, stop TB introduced, we prefer to have even better data deeper data and then we'll engage them. But those are partners of Qiagen for so many years. Remember, back in 2015, when WHO stated that latent TB was a key asset in the fight against active TB, it was after discussion and work with Qiagen.

Then to stay also again with the AI tool. The question is, when is the launch date? Is it any -- a bit more -- let's be a bit more specific on the software for predicting tuberculosis. And also, is it exclusively for QuantiFERON and DiaSorin customers who can benefit from that AI risk certification tool that we're launching.

I would invite Nitin to take that question, Nitin, on the approximate launch date and on which kind of workflow we want to adjust that tool.

Yes. I mean, again, that the tool is very specific to QuantiFERON because, again, it requires both CD8 and CD4 and it requires access to this longitudinal information that we have collected now through this [ 13 million ] data sets -- for over a decade. So very specific to us. And I just want to highlight that we have a very cross-functional team working on this. We have experts in the QuantiFERON chemistry clinicians or medical experts also working with us. So it's a very cross-functional effort. And the goal is to get the test out as quickly as possible. We're targeting 2027 for the launch of the two.

Nitin mentioned CD4, CD8, and we have a question around that. So what advantages does the CD4, CD8 base latent TB tests have?

Nadia?

Yes. Thank you very much. So I'm going to give the basics and then afterwards, I'm going to invite Paranpal to continue. As a company, Qiagen decided to launch a fourth generation. we were already in the market for some time, and we knew very well why we decided this unique CD4, CD8 combination because we wanted to improve, and we wanted to put the standard again a little bit higher. So what we see today is, and we see this from all the publications that are out there. that with a combination between CD4 and CD8, you have a much more solid test and your results are much more reproducible. So I don't know, Parampal if you want to add something on the science part.

Sure. Thank you, Nadia. So the CD4 cells are available, T cells are available when there is a response against TB antigen. However, when there is a patient population, which is immunosuppressant, their CD4 cells response could be impaired. In that situation, it's so important to have another T cell response marker, which is CD8, which allows us to look at more biologically relevant information on those patient populations, which are high risk.

And if you look at the TB case management, these are the groups who are more prone to get from a TB infection to TV disease. This is why a combination of CD4 and CD8 allows us to have more sensitive and specific test which people can rely on patients can rely on clinicians can rely on and the laboratories can rely on. So this is the uniqueness of CD4 and CD8, which is evident -- so much evidence is available through publications, which allows us to really be proud as a Qiagen to have a very strong test on the market.

So now 1 question again on automation, which is Tecan Hamilton. So just to clarify that, are we still offering -- is there still a partnership with Tecan Hamilton with the impact of system that we're going to launch.

But we need to be clear. What is the power of automation? It's obviously ease of use, gaining time, gaining efficiency, cost efficiency, patient efficiency. But the power of automation -- automation is also in flexibility. It's not one size fits at all. And therefore, we want to continue to offer the QuantiFERON as it is, the QuantiFERON on LIAISON. Nadia spoke about the conversion progressively to the CLIA2 on LIAISON. Some customers are only sometimes interested in the front end, and they are used to work with Tecan. It's going to continue.

The same with Hamilton. Some customers would say, I take care of the front end, I have the technicians for that. And I just want the liaison automation. That's perfectly fine. It depends on volumes. It depends on throughput. It depends on the country. But something I would like to ask also Nadia to highlight is that even our full automation with Inpeco Peco will be flexible.

Yes. Thank you very much, Thierry, indeed. So we really need to give an answer to the needs of the customer if you have a small customer or to a higher customer. And I think a lot of people if they see Inpeco, so we have different possibilities.

The 2, so the [ alicator ], and we have our incubator. And alicator will be needed if a customer works with a 1 tube format. An alicator will not be needed if a customer works with a forte format. So this is already a tailor-made solution. You have an incubator depending on the volume you're going to be able to have a day, you can put in multiple incubators one besides the other.

And you could, in principle, also build on a current street that is already available in labs. So we really go from a tailor-made solution because when a customer wants to go for automation we make a group we sit down with the customer, and we make together with Inpeco, together with [ Asuran ] and us, we make a tailored proposal to the needs of the customer.

Also keeping in mind that sometimes customers can grow -- so if a customer would grow in their volume, there's always a possibility to add an extra VSO instrument or to add the next incubator.

And on volume, which customers would benefit from an end-to-end workflow from an end-to-end automation? Is it more targeted to high-throughput customers. So just maybe a bit more color on that.

So it's really targeted for what we call our high-end customers. But don't be blind. This is not only U.S.-based customers. So worldwide, we have quite a lot of customers that have a possibility to go into this automation process. These are customers that today we would like to serve in a way that is unique in the market.

Okay. I'll jump back to AI. We have a couple of more AI topics. Why does risk stratification matter? And isn't it the point to treat all patients? And just what's the added value for that?

Because we tried to explain, especially also a year ago during our deep dive that when you have such a reservoir of potentially activity. We said 2 billion, 1/4 of the world population, which means probably that in this room, there is someone who is let anti positive. We like -- but that's the way it is. 2 billion people. It is clear that from cost management from, I would say, personalized medicine standpoint. Having the ability to detect or to predict who in dose latent TB has the highest score to go to active TB, therefore, needing a specific follow-up, a longer treatment specific attention and complete adherence because that's the problem many times with the patient. They do not comply sometime with their treatment. It's key.

Many companies have been training and Qiagen as well with different technologies for many years to get there with protein-based option with genomic-based solution. It failed all the time. And suddenly, we realize, wait a minute. These companies have multiyears of -- multiple results. And we have also acquired all other health care data and now we are creating those algorithm.

So now let's see -- let's take a financial one in between. It's on our 2028 target of $600 million. What gives us confidence in that? And also how the new launches are contributing to that?

So that's a very fair question. Back in our -- back to our Capital Market Day in 2024. We set the target of $600 million, as we said, Domenica, for 2028. We were very transparent to -- the market as well that if all the other applications on QuantiFERON are growing in a healthy way, we suffered the loss of 1 market, especially in the U.S. and in some countries in the Middle East, but mainly in the U.S., it's the immigrant mark.

And we gave the market a very clear indication. We believe it's between $30 million, $35 million of impact. We still believe that because of the potential of new applications, not only with what we are launching today, but existing immediate opportunities thus testing for patients under dialysis, for example, extending the knowledge around, for example, the connection between diabetes patient and -- tuberculosis that we have ways to mitigate. But at the moment, let's execute on our target for this year, let's execute on coming back to growth with QunatiFERON in H2 and we'll come back with the appropriate target. What I keep in mind is that the market to convert is still significant. This market is still growing. It's a good market to be, and we have more and more solution to address it completely.

And yes, on the conversion rate of the market, we keep saying 40% already converted? What do we need to get this conversion rate above 50% and even higher? And how might new entrants impact this conversion dynamics.

Nadia, do you want to take it? -- if you want.

So on the conversion rate, it's a combination between our sales teams, our clinical demand teams, but also our medical teams. Because Thierry just mentioned that there is new groups of patients that have the possibility to be tested. And this is really where our medical affairs does a huge soda. So our teams have strict criteria. We follow up. We go to patients, and we continue repeating the same message.

Key message, if you want to convert a skin best to a blood-based IGRA test is, everybody who's BCG-vaccinated will quite often be false positive -- in test. So you can't really deal with it. Secondly, when you do a skin test, people need to come back twice. So these are the messages that we continue seeing and we see year after year that a big part of the market is shifting.

Some parts of the market have almost shifted 100%. If you look to biologics. Biologics is almost using blood-based IGRA test and QuantiFERON test for all of their patients. If there is a new company coming into the market, this new company together with us, can move the 75 million that is today the market of latent TB up to 80 million, up to 90 million because Thierry just said, there's 2 billion people with latent TB. So the number of 75 million is much higher because in some countries, now that everybody has tested.

In addition to that, I would like to add that back in 2016, when we deliberately choose DiaSorin as a partner, it was a very forth, well for choice. DiaSorin is not just an immunoassay company. Talasorin is a leading company in esoteric added value medical test. Their salespeople like Qiagen salespeople, they are used to spend 5, 6, 7 visits to convert to customers. We like it or not. Health care is very prone to innovation, but sometimes there is a lot of conservatism. So for example, in the U.S., we exactly -- we have a tool, a marketing tool, and discuss that with the market over the last 3 years. We have a marketing tool, enabling us to know by ZIP code where the remaining skin test customers are -- and then once we have the information, we look at what kind of population are they basically serving immuno conference and we try to convert them.

But it takes some time up to 6, 7. It's fair to say that it takes on average 7 visits to convert not because they are not convinced, they are, but because they are comfortable with the way it works. My technicians are trained, and little by little, you go to medical value, you go to cost efficiency and they move to you. That's a natural movement, but it takes time. It takes time. It takes medical and it takes experience and mindset. This is why DiaSorin was not just an option among it was the option to partner efficiently with us.

Let me bundle a couple of questions on the Inpeco system. So that's moving again. So where do you find Inpeco systems and what type of labs? Are these new call points for QuantiFERON? Are there customers that have seen us? How is the response of customers?

So I quickly say I'm going to move to Riccardo because nobody can speak better about where Inpeco is in the world. But yes, obviously, the major labs in the world are all customers of QuantiFERON as we speak. And obviously, we have visited already some of them with a fantastic basically attention. They saw the workflow. They also suggested some improvement and its work ongoing, but it's very exciting to see the level of interest, the fact that they come back to us when is it going to be available? We already have customers saying, I want to be the first one to implement it. But Riccardo, what about the presence of Inpeco all over the world.

Yes. We are present almost in every country in the globe. We have currently around 3,000 automation tracks installed worldwide. But I think the important message is that, obviously, we are perceived as a company working in the high-end segment of the market. You mentioned the quest, the LabCore all the biggest labs across the globe have our automation. But 80% of our automations are in the smaller type of lumps. Because I was hearing Nadia loud and clear. Obviously, we are now targeting high-end segment, but there is a huge portion of the market that is not only looking just for efficiency gains, but we're also looking to really remove previous manual operations. So these kind of labs are really in a search in a quest for end-to-end automation. And this is where I see our partnership coming together.

Global leader in lab automation, the global leader in tubercolosis, latent TB testing coming together with, as you said, the super performance analytical platform like the LIAISON from DiaSorin, I really think we are bringing something really impactful in the market. And we have a huge market target. As I said, 3,000 installations across the globe that can plug in this new solution. from our 3 companies.

Thanks, Riccardo.

And on the DSR and chemistry. So what is the feedback from customers? Are we seeing any faster adoption or transition to LIAISON. And how did this address any hesitation and conversion?

So we have given numbers today. Nadia can repeat them. And yes, the reception in Europe is very good, but we just got to prove to the FDA in the U.S. So we are currently introducing to the customers. But Nadia?

Yes. Thank you very much, Thierry. So the feedback of the customers is really overwhelming because we know it goes faster. We can -- we have a faster time to detection. We can do much more patients. And what is ongoing now is we're in a transition plan. This transition plan is really followed up extremely correctly. And we haven't really had 1 customer that was not pleased with the results of the CLIA2. So we are following the conversion plan, and we are convinced that it will be done on the timing that we have for some.

And now the last one for today. So the full automation workflow can it also be used with other latent TB tests blood-based latent TB test? Or is it really just available for QuantiFERON?

I think we did answer, but it's a good question. Obviously, it's a key question. We did answer Riccardo and I and Nitin said the word also about this. it's a purpose-built automation for QuantiFERON. I believe that if those partnerships want to be winning partnership, there needs to be a kind of call it exclusivity or call it special relation, but something very strong.

Basically, we like the fact that Inpeco is so specialized into very precise automation. We like the fact that DiaSorin is so specialized into esoteric testing, and that makes that specialization and that depth of partnership because we all have skin in the game that makes this partnership potentially successful.

And with that, we are at the end. So any closing remarks.

No, I would like to take advantage of meeting being with us. He's heading our portfolio development to give his vision as a concluding words. And obviously, thank Riccardo, thank Paranpal. Thanks, Nadia. Thank you, Domenica, thank our IR team. But Riccardo, thanks a lot for being with us. And thanks also to DiaSorin -- if they are not with us today, we thank them for this partnership. Nitin?

Yes. Thank you, Thierry. So I hope what all of you saw in today's program is not just a product update. It's an ecosystem. That's what we are building, and we're building that from a position of strength. So 3 things. First, we're making the tests faster. 75% more testing to CLIA2.

Number two, we're making the test fully automated, no manual steps. And number three, we're adding intelligence to the test on the basis of 13 million patient records that no one else on Earth has. That's ecosystem leadership. That's what today is all about. Thank you.

Thank you, Nitin. And with that, we are at the end of the spotlight session. Thank you for your participation. Hope to see you soon again. And if you have any remaining questions, please always feel free to contact us. Happy to help you. So see you then. Bye-bye.

Ladies and gentlemen, thank you for standing by. I am Katie, your call operator. Welcome, and thank you for joining QIAGEN's Preliminary Q1, 2026 Earnings Conference Call Webcast. [Operator Instructions] Please be advised that this call is being recorded at QIAGEN's request and will be made available on their Internet site. [Operator Instructions]

At this time, I'd like to introduce your host, Daniel Wendorff, Vice President, Head of Investor Relations at QIAGEN. Please go ahead.

Thank you, Katie, and welcome to our call on our preliminary results for the first quarter of 2026. In light of the update to our 2026 outlook, the pre-announcement was issued in line with German disclosure requirements yesterday evening. We are planning to publish full Q1, 2026 results on May 6, 2026. We appreciate your time and interest in QIAGEN.

Joining the call today are Thierry Bernard, our Chief Executive Officer; and Roland Sackers, our Chief Financial Officer. Also joining us is Dr. Domenica Martorana from our Investor Relations team. As always, today's call is being webcast live and will be archived in the Investor Relations section of our website at www.qiagen.com, where you can find the press release and presentation accompanying this call.

Please also note that this call will include forward-looking statements. Actual results may differ materially from those projected due to a number of factors outlined in our most recent Form 20-F, and other filings with the U.S. Securities and Exchange Commission. We will also refer to certain financial measures not prepared in accordance with U.S. generally accepted accounting principles, or GAAP, that provide additional insights into our performance. Reconciliations to the most directly comparable GAAP figures are in the release and presentation. All references to earnings per share refer to adjusted diluted EPS.

With that, let me hand the call over to Thierry.

Thanks a lot, Daniel, and good morning, good afternoon or good evening, depending on where you are in the world. Thank you for joining us, and thank you also for your interest in QIAGEN.

As you saw in our announcement for our preliminary results for the first quarter of '26, we delivered strong profitability as adjusted diluted EPS achieved the outlook despite mixed sales results. Sales were below our target due mainly to significantly lower QuantiFERON immigration testing demand and continued caution among U.S. Life Sciences customers. The important point, however, is that 4 of the 5 pillars achieved or exceeded our expectation, and we do continue to believe in the long-term opportunities for QuantiFERON. While we are taking a prudent approach to the updated outlook, we see tangible drivers for stronger growth trends in the second half of the year. Let me now highlight some key messages.

First, we delivered adjusted EPS of $0.54 at constant exchange rates, in line with our outlook despite mixed sales trends and a tougher macro environment. Net sales were $492 million, up 2% on a reported basis, but down 1% at CER, and below our outlook for at least 1% growth CER. This reflects a mixed performance with solid momentum across many areas of the portfolio, offset by the weaker-than-expected QuantiFERON sales. Despite the lower sales, disciplined execution supported earnings and enabled us to deliver on our adjusted EPS outlook.

Second, our growth pillars delivered a solid performance with 4% increase of sales CER. Sample Technologies grew 9% at CER, and also rose 3% CER excluding the Parse acquisition. QIAcuity delivered double-digit CER sales growth on gains in both consumables and instruments. Our bioinformatics business, QIAGEN Digital Insights, delivered solid single-digit CER sales growth, led by growth in clinical applications. And [ QIAstat Diagnostics ] sales declined 1% CER, facing a tough comparison to a stronger prior year quarter. At the same time, for QIAstat, consumables were up on double-digit growth for GI and meningitis panels, where instrument placement continued at a growth at a good pace.

As I mentioned at the start, QuantiFERON sales declined and those were down 5% CER. This was mainly due to significantly lower immigration testing demand in the U.S. and in the Middle East. This impact is exclusively isolated to immigration-related volumes. We did not see changes in pricing, competition on -- or underlying demand in the key patient testing markets. We continue indeed to see stable ordering patterns and solid growth in the remaining 90% of the QuantiFERON business.

As we have said before, the underlying market for latent TB testing is growing at about 4% to 5% annually, and we now see the U.S. market growing about 1 percentage point lower at this time due to the immigration situation. Overall, we expect sequential improvement over the course of the year for QuantiFERON testing.

Third key message. We maintained a high level of profitability in the first quarter with our disciplined approach to managing the business and making value-creating investment. The adjusted operating income margin is expected to be at about 27.4%. This reflects continued efficiency gains while absorbing headwinds from tariff and currency, as well as the impact from the Parse acquisition.

Fourth, we have updated our outlook for 2026 to reflect those developments and a more cautious macro environment. Net sales 2026 are now expected to grow about 1% to 2% CER, with adjusted diluted EPS expected to be at least at $2.43 CER again. The updated outlook reflects lower expectation for QuantiFERON, continued caution among the U.S. Life Sciences customers, volatile OEM customer ordering trends and ongoing geopolitical uncertainty for 2026. At the same time, we see very tangible reasons for faster sales growth of about 4% CER in the second half of 2026. This includes the end of headwinds from the discontinuation of NeuMoDx and DIALUNOX, benefits from new product launches, a sequential improvement in QuantiFERON and better-than-expected contribution from Parse, and last, a modest improvement in Life Sciences demand.

With that, I'll hand it over to Roland for more details on the financials.

Thank you, Thierry, and good morning, good afternoon. Let me now take you through the financial details behind this announcement and let us through our updated outlook.

As Thierry said, Q1 was a mixed quarter. We hit our outlook for adjusted EPS through disciplined execution, while sales were slightly below target. For Q1, the preliminary net sales of USD 492 million were up 2% on a reported basis and down 1% on constant exchange rates. The positive impact of about 3 percentage points on sales at actual rates was in line with our planning. Same was the case for adjusted diluted EPS of $0.54 on a reported basis, and $0.54 at constant exchange rates, in line with our outlook.

Let me now review the sales results. Sample Technologies delivered USD 170 million of sales, up 9% CER compared to the first quarter of '25. Excluding the Parse acquisition, which is performing very well, the sales rose 3% CER. Growth was supported by demand for automated consumables and instrument placements, as we saw good trends worldwide. In Diagnostic Solutions, sales were USD 185 million and down 4% CER. The main driver here was a 5% CER decline in QuantiFERON sales, which overshadowed solid trends in many patient testing groups.

QIAstat-Dx sales were down 1% CER, which was expected given the tough prior year comparison to a period with a very strong respiratory season. Diagnostics Solutions also included a year-over-year headwind as expected from the mid-'25 discontinuation of the NeuMoDx system. PCR nucleic acid sales declined 13% CER to USD 69 million. With this product group, QIAcuity delivered double-digit CER sales growth. However, we also saw significantly lower sales in other areas, including PCR consumables and the OEM business as we felt the impact of life science funding constraints. And in the Genomics / NGS product group, sales were up 4% CER to USD 57 million. This was supported by QIAGEN Digital Insights, which grew at a solid single-digit CER pace, driven by growth in clinical bioinformatics.

Let me now turn to profitability. We are expecting adjusted operating income margin of about 27.4% in the first quarter of '26, supported by ongoing efficiency gains as we absorb the impact of tariffs and currency movements while also investing into the future of the Parse single cell-analysis business.

With that, let me hand back the call to Thierry.

Thanks a lot, Roland. Let us step back a bit for the quarterly numbers and share a few reasons why at QIAGEN, we continue to feel confident about the portfolio and the path to stronger growth. The message here is that our pillars continue to move ahead and only the 2026 sales target for QuantiFERON has been adjusted.

As we mentioned earlier, the issue with QuantiFERON is isolated to immigration demand. Importantly, this does not change our view of the long-term opportunity. Trends in other patient testing groups remain solid, and the underlying market for latent TB testing continues to grow. As you have probably seen, new data published around World Tuberculosis Day further reinforced the role of QuantiFERON in detecting latent TB infection, particularly in high-risk and immunocompromised population. We are also advancing scalable laboratory workflows for QuantiFERON. A new generation of chemistry for QuantiFERON detection on LIAISON system with our partner, DiaSorin is now being rolled out in the U.S., in addition to the earlier launch in Europe and other areas of the world.

We are also seeing targeted screening initiatives ramp up in various patient groups, diabetes or dialysis, particularly as well those being prescribed biologic therapies and immunocompromised individuals. Looking ahead, we will host a virtual QuantiFERON spotlight session on May 7, where we will provide you with more details on our strategic priorities, workflow automation plan and the additional enhancement that underscore the long-term opportunity of this product.

Turning to sample technology. This remains one of the clearest example of the portfolio moving ahead as forecasted. We continue to advance our automation strategy with our 3 new system launches for 2026 moving ahead and receiving positive customer feedback. As an example, QIAsprint Connect was launched in February, and we are very encouraged by the first wave of orders, with the first sales contribution expected in the second quarter. We also have the first orders for QIAsymphony Connect after the launch in late 2025. Full IVD commercialization remains on track to begin in the middle of this year. QIAmini is also on track for launch later in 2026.

We continue to see good traction in strategic high-value areas such as liquid biopsy, where QIAGEN system are being integrated into the workflows of major players. The Parse business is also performing better than expected, and we are on track to exceed the '26 sales target of about $40 million. As you remember, Parse gives us an entry into single cell analysis, a highly attractive area where researchers need scalable workflows and high-quality data generation. This was also reflected at the recent AACR Cancer Research meetings where we showcased application across our oncology workflow. This includes our expanding capabilities in sample preparation, single cell analysis and digital insights. For QIAcuity, we continue to see strong momentum in digital PCR. Our focus, as you know, this year includes expanding applications such as gene expression while continuing to develop a portfolio of companion diagnostic with our pharma partners.

Turning to QIAstat diagnostic. We continue to broaden the panel menu and strengthen the platform for syndromic testing while also advancing our pharma partnership in companion diagnostic. In the first quarter, for example, we received U.S. clearance for the GI panels on the QIAstat Rise, which is, as you remember, the high throughput version of this modular system. We now have the respiratory and GI panels CLIA for the Rise version.

QIAstat is also being expanded into bloodstream infection testing. In Europe, we launched the first of the new blood culture panels in January. We also submitted the first panel to the FDA, and we are awaiting a decision. This marks a very important expansion beyond respiratory, GI and meningitis to support better, faster clinical decision support. Finally, QIAGEN Digital Insights, our bioinformatics solution, continues to strengthen our Sample to Insight strategy with its status as a leader in bioinformatics. Within QDI, clinical bioinformatics remains the key growth area, double digit in this first quarter, as we are building capabilities through the integration of the Franklin platform from the recent acquisition of Genoox. So across those areas, the message is very consistent. We are addressing the QuantiFERON immigration testing demand issue, while the rest of the portfolio moves ahead as planned.

And now back to Roland to discuss our outlook.

Thank you, Thierry. Let me now provide some additional perspectives on our outlook for '26 and for the second quarter.

As we have said, we are taking a prudent approach to reflect the development in the first quarter and the current macro environment while remaining focused on delivering solid profitable growth. For the full year '26, we now expect net sales growth of about 1% to 2% at constant exchange rates, compared with our previous outlook for at least 5% CER growth. Adjusted diluted earnings per share are now expected to be at least $2.43 at CER, compared with our previous outlook for at least $2.50 at CER.

The updated outlook reflects two main factors. First, QuantiFERON sales in '26 are now expected to be steady at a CER basis at around USD 500 million. This compares with our previous target for about 6% CER growth, or about USD 535 million. We have reduced these expectations in light of the immigration testing demand trends. This customer group represents about 10% of total QuantiFERON sales, or about USD 50 million. We reduced this by about USD 35 million for '26, and we have not seen changes in demand for the remaining USD 15 million, which is largely European immigration testing. This impact from QuantiFERON reflects about 1.5 percentage points of headwinds to full year '26 growth compared to our prior year outlook.

Second, we are taking a more cautious view on mainly U.S. Life Science customer spending for a total of about USD 40 million, or about 2 percentage points of headwinds. This involves 3 components. About $15 million to $20 million of headwind comes from research customers in the U.S. Another $20 million comes from volatility in customer ordering in our OEM business, which also includes government agencies in the U.S. And lastly, a few million dollars of pressure comes from the Middle East conflict and the broader geopolitical uncertainty that has developed since the start of the year.

Turning to the second quarter. Net sales are expected to decline approximately 2 percentage points CER compared to $534 million in Q2 '25. These sales trends take into consideration that QuantiFERON sales continue at a largely unchanged level from the second quarter of '25. While we believe in the full year target for QIAstat-Dx sales, we have purposely taken a more conservative view on these product sales for the second quarter in light of the strong year ago comparison. The pillars as a group are expected to grow about 4% to 5% CER in the second quarter, compared to the 4% CER growth in the first quarter of the year. And as a reminder, the second quarter will be the last period with headwinds from the discontinuation of NeuMoDx and DIALUNOX.

For adjusted diluted EPS, these are expected to be at least $0.60 at CER in the second quarter compared to $0.60 in the prior year period. Operational efficiency and disciplined cost control remain a key priority for QIAGEN and continue to support profitability despite lower expected sales. At the same time, earnings in Q2 will absorb a dilutive impact of around $0.01 from the Parse acquisition.

Let me now address 4 drivers for faster sales growth in the second half of about 4% CER. First, about 2 percentage points of incremental growth come from the roll-off of headwinds from the discontinuation of NeuMoDx and DIALUNOX and unchanged from our prior expectations. Second, about 2 percentage points are expected to come from new launches, including the sample prep instruments and additional offerings for QIAstat-Dx and QIAcuity. This is also unchanged from prior expectations. Third, about 1 percentage point is expected to come from improving year-over-year growth from QuantiFERON as we anticipate growth in the second half of '26 compared with the first half. Finally, about 0.5 percentage point of improvement is expected from a combination of the past acquisition, transforming better than our target for about $40 million of sales in '26, and modestly better trends in U.S. Life Science funding as the year progresses.

Taken together, these factors explain the expected bridge from sales declining about 1% to 2% CER in the first half to a growth rate of about 4% CER in the second half to reach our target for about 1% to 2% CER growth in the year overall. And looking ahead, in terms of midterm growth, we see very positive trends for QIAGEN as we work through a period of rebasing QuantiFERON demand. The pillars of the group are expected to grow about 7% for '26, and we see this continuing at a healthy pace in the future and supported by QuantiFERON returning to a more normalized growth rate in '27.

With a series of new product launches on the way, in particular, the new instruments and sample technologies, this provides even more confidence in delivering faster sales growth. The pillars are also increasing as a share of total sales. They are now at about 75% of total sales and rising, and we are taking actions to stabilize the base business.

Let me also briefly address currency trends. For the full year, we currently expect a tailwind of about 1 percentage point on sales, and a neutral impact on adjusted EPS. This is unchanged from our previous assumption. For Q2, we expect a tailwind of about 1 percentage point on sales and a neutral impact on adjusted EPS. Overall, we have taken a prudent approach in updating our outlook, reflecting current market conditions and known headwinds. At the same time, we remain focused on disciplined execution, protecting profitability and returning to growth in the second half of '26. Last but not least, we also confirm our adjusted EBIT target of 29.5% CER for the full year.

I would like now to hand back to Thierry.

Thank you, Roland. And before we go to the Q&A session, let me go over a brief summary of this call today. Q1 was a mixed start to the year, but we delivered adjusted EPS in line with our outlook through disciplined execution. The sales shortfall was driven mainly by the QuantiFERON immigration testing demand reset, and we are addressing this directly and proactively. We continue to view this as a rebasing of demand in this testing group, but absolutely not a change in the long-term opportunity for latent TB testing. Trends in all the patient testing groups remain solid, and we expect sequential improvement during 2026.

The rest of the portfolio continues to execute on target. Sample Technologies, QIAcuity and QIAGEN Digital Insights delivered solid growth in this first quarter of 2026. New product launches and portfolio additions support our confidence in stronger growth trends in the second half. We have updated our 2026 outlook to reflect what we are seeing in QuantiFERON immigration testing trends, as well as ongoing caution among U.S. Life Sciences customers and the broader macro environment. But at the same time, we see tangible reasons for faster sales growth in the second half of the year.

So in closing, we are updating expectations prudently, and we are staying really focused on delivering solid profitable growth.

With that, I'd now like to hand back to the operator for the Q&A session. Thanks a lot.

[Operator Instructions] The first question comes from Michael Ryskin with Bank of America.

Great. I appreciate the color you provided on the slide deck and on the call. I want to dive into a little bit more of the difference between what you saw in the first quarter versus how you're updating the guide.

If we look at your reported results for the quarter, you missed consensus by about $9 million, $10 million. And if we look at QuantiFERON at down 5% CER, it seems like the majority of the miss was specific to QuantiFERON, maybe $8 million of the $10 million was QuantiFERON. But then for the full year guide update, $35 million is QuantiFERON, but $40 million is that U.S. Life Sciences. So I want to really focus on that. Just didn't seem like it was that much worse in the quarter itself. So is it something that deteriorated in March later in the quarter? Is it order trends you're seeing? Just you commented $15 million, $20 million from research customers, $20 million OEM. Just didn't really seem like that played out in the quarter itself. So why is a steep revision to the full year guide there if you didn't see it in 1Q?

So thanks a lot, Michael. And I think that you are nailing it indeed for the first quarter. Out of the $10 million shortfall, QuantiFERON indeed represent at least $8 million of that. Now for the full year, we take a realistic but also cautious view based on many factors. We believe indeed, as you said, that the total impact, rebased on an annual basis for QuantiFERON immigration testing is around $35 million. In addition to that, we take a cautious approach to the current U.S. Life Sciences customer environment and kind of wait-and-see attitude that we have seen in the quarter 1. This represents roughly $20 million of cautious expectations.

And then we also take -- and this is not new, if you remember our previous call, a prudent approach for our OEM activities. By definition, OEM activities are more volatile because they are based on deliveries of big bulks of product one time. And so year-on-year, you have that volatility. And for the year 2026, we believe it's another impact of around $15 million to $20 million. So overall, between QuantiFERON immigration testing and those 2 events, cautious Life Science kind of wait-and-see attitude, especially in the U.S. and OEM, you get the difference to the re-forecast for the year.

Okay. All right. I appreciate that. And then for my quick follow-up, on QuantiFERON itself, you kind of alluded a couple of times on the call to this is a rebasing year, and you expect it to improve in the second half and you expect it to improve going forward.

Just sort of what gives you confidence in that? You saw QuantiFERON already slow a little bit in 4Q '25 to about 5% CER. Why do we think QuantiFERON is going to reaccelerate? Why isn't this a low to mid-single-digit grower going forward, given the robust growth you've had over many years and the fact that some of these immigration pressures are very likely to persist?

A fair question. You can imagine, Michael, that we have done a lot of analysis of the most -- in the most recent weeks. And this is why we came to the conclusion that it's an immigration isolated event. And we don't imagine and we don't expect this event to happen again with the same magnitude in 2027, for example.

The reason is very clear. Once you have reset the basis because you have lost a market of immigration that you are not going to test anymore, the impact on the following year, obviously, is not happening with the same magnitude, first. Second, because when we look at other applications for QuantiFERON, immunocompromised patients, diabetes patients, dialysis patients, for example, we still see very good growth. And so to give you precise numbers internally, but also with external experts, we have analyzed again our growth expectation for this market. And the conclusion is the following.

In most of the world, the testing demand for latent TB continues to grow at around 5%. In the U.S., you indeed lose that immigration testing base, but the rest of the market continues to grow at around 4%. So it's still a healthy market to be. The second reason why we are confident, and this is why I confirm our invitation for the spotlight session on May 7, is that we continue to invest on this range of products. We have a new, more efficient workflow together with DiaSorin is that we call -- is what we call the CLIA2. And on May 7, we are going to show you enhanced automation investment and also progresses into patient scoring to show that we have still a potential to target probably around 5% growth for this range of products.

We will take our next question from Tycho Peterson with Jefferies.