Revvity, Inc. (RVTY) Earnings Call Transcript & Summary
September 9, 2026
What were the key takeaways from Revvity, Inc.'s September 9, 2026 earnings call?
In the second quarter of fiscal year 2026, Revvity, Inc. (RVTY:US) reported revenues that met expectations, with notable strength in its Diagnostics segment, particularly in reproductive health and immunodiagnostics. The company also announced a tuck-in acquisition of Human Cell Design, enhancing its reagents business. Management signaled optimism regarding the recovery in the pharma biotech sector, indicating a potential resurgence in orders driven by increased customer engagement and investment in new technologies, including AI. Revenue guidance for the remainder of the year remains stable, with expectations for continued improvement in the Life Sciences segment.
What topics did Revvity, Inc. cover?
- Acquisition of Human Cell Design: Revvity announced a tuck-in acquisition of Human Cell Design, which fits well with its reagents business and enhances capabilities in preclinical to clinical transitions. CEO Prahlad Singh stated, "Human Cell Design is a great tuck-in acquisition for our reagents business."
- Strong Performance in Diagnostics: The Diagnostics segment outperformed expectations, particularly in reproductive health and immunodiagnostics. Singh noted, "Diagnostics did slightly better than what we had, both reproductive health had a great quarter."
- Pharma Biotech Recovery: Management expressed optimism about the recovery in the pharma biotech sector, attributing it to reduced uncertainty and increased investment. Singh mentioned, "the calming down of the chaos allowed for pharma biotech customers to start planning and reinvesting back to what pretty much normal should look like."
- AI's Role in Growth: AI is expected to drive incremental investment and growth in drug discovery. Singh stated, "the AI component is not taking money out from left pocket and putting it in right pocket. I think it's incremental investment that is going to go on."
- Software Segment Performance: The software segment faced challenges, with a 20% decline year-over-year, but management remains optimistic about future growth driven by new product launches. Singh indicated that the software business is expected to grow in the low double digits in the medium to long term.
What were Revvity, Inc.'s September 9, 2026 results?
- Revenue: $X.XB (in line with expectations)
- Diagnostics Revenue Growth: mid-single digits (strong performance in reproductive health and immunodiagnostics)
- Software Revenue Decline: -20% (compared to previous year, tough comp)
- High Content Screening Contribution: 1/3 of platform business (increased from 1/4 previously)
- Margin Guidance: low 30s in Q4 (raised guidance twice this year)
- Immunodiagnostics Growth: double digits ex China (consistent performance since acquisition)
Revvity's strong performance in Diagnostics and the positive outlook for the pharma biotech sector are encouraging for investors. However, the challenges in the software segment and the anticipated slowdown in reproductive health growth present risks. Key catalysts to watch include the successful integration of the Human Cell Design acquisition and the impact of new product launches in the software segment.
Earnings Call Speaker Segments
Evan Stampler
analystAll right. Great. Welcome, everybody. Today, we have Prahlad Singh, CEO of Revvity. And maybe I'll just let you start. I mean, you did announce a small tuck-in acquisition this morning. Maybe I'll let you kind of explain what you bought, how it fits in your portfolio and maybe what it let you do that you couldn't do prior.
Prahlad Singh
executiveYes. Good morning, Evan. Thank you for inviting us. I think as we've talked about, Human Cell Design is a great tuck-in acquisition for our reagents business, and it fits perfectly well with what we've talking about how our reagents business has been doing good on the preclinical stage. As you go from preclinical to clinical, you go through looking at tissue culture, cell culture, cell lines and human cell designs that are as close to looking at humans possible. And going through this process, the Human Cell Design portfolio fits very well in our reagents business, and I think it will be a great tuck-in acquisition.
Evan Stampler
analystGreat. So H 2Q, it sounds like things are generally in line with expectations. Life Sciences, maybe a little bit weaker than expected, stronger in Dx, but you also had some -- I think you also had some I guess you weren't able to fully meet demand on some of your high-content screening. So maybe just walk us through the quarter and how it played out versus expectations.
Prahlad Singh
executiveYes. I think 2Q, as we've talked about on the earnings call, it played out pretty much as we expected. I think as you said, Diagnostics did slightly better than what we had, both reproductive health had a great quarter. Immunodiagnostic did very well. On the Life Sciences side, software was as expected as we had forecasted. Instruments on the platform side, we've got a very strong backlog. And on the reagent side, we were low single-digit growth. So it's pretty much played out with a little bit of nuance up and down here and there, but pretty much along what we had thought it would do.
Evan Stampler
analystGreat. Okay. I mean going into pharma biotech, I think it was down mid-single digits. positive ex software. I mean the commentary did seem to be a little bit more optimistic, I think, than -- or constructive than it has been in the past. Are you seeing that the -- that you're having conversation with customers and where the budgets are actually turning into orders? And is this revenue -- is more likely to impact later this year or more into '27?
Prahlad Singh
executiveYes. I think pharma biotech, the phenomenon has not been just from the last quarter. I think I would say there was a lot of uncertainty last year that carried into 2025 that came from a bunch of issues, whether it was tariffs in, tariffs out. I think for us, what we use as a marker is the meeting of Pfizer at the White House sort of was somehow a key point in the turn and then brought certainty into the investments and the spending and then sort of it brought through a start of the resurgence of pharma biotech after a prolonged period of time. And I think the calming down of the chaos allowed for pharma biotech customers to start planning and reinvesting back to what pretty much normal should look like. And I think we've seen that continuously over the past several quarters where the investment in pharma biotech is gradually coming back to what normal should look like. And then I think it's going to continue to play out, especially now with the sort of resurgence and or the engagement that we are seeing with new modalities and technologies such as AI playing a role. So that is adding an added resurgence to the end market.
Evan Stampler
analystHelpful. And we just have Bruker up here. And I figured I'd ask you this too because you guys talk a lot about AI. They made a comment that they think that AI spending has likely impacted to some extent, normal spending on life science tools, your more traditional life science tools.
Prahlad Singh
executiveDo you sign on to that?
Evan Stampler
analystMaybe it's not your high-content screening, maybe other parts of your portfolio where there's just been a reallocation of resources maybe this year that will translate into more demand maybe for your tools next year or '28 as they look to train their models that they've been.
Prahlad Singh
executiveYes, we don't believe so. I mean from our perspective, I think the pharma biotech end market coming back to normal was more of a consequence of the calming down of the chaos and uncertainty and the reinvestment back because you've got to have investment in preclinical and you've got to have the innovation because of all the patent cliff issues that the pharma biotech companies are facing. So from our point of view, we see that as more of a normal course of investment coming back. I think the AI component is not taking money out from left pocket and putting it in right pocket. I think it's incremental investment that is going to go on and is the beginning of it to accelerate drug discovery and development. And I think this is -- as we've talked about, if you go back and listen to what we -- Max, Steve and I have been talking about from the beginning of this year at investor conferences in our 1Q call and our second quarter call as to how this is playing out. And it pretty much is playing out as we had hoped and forecasted.
Evan Stampler
analystThat's great because no one's been able to forecast. makes me even more impressive. But you're right, you guys -- like I said earlier, you guys have been talking about this and kind of leading the discussion, I think, within the life science tools space. So it's nice to see it kind of play out. I mean, sticking with that theme, high content screening was a really big part of the conversation on the 2Q call, I spent a lot of time on it. Maybe talk about how big that business is for you right now? What the funnel looks like there? I know you -- like we talked about earlier, you did have some capacity constraints, which I believe are just are pretty easily fixed by just adding more people. But yes, just tell us about what your -- what the funnel looks like there and maybe what that -- down the line, what that could potentially mean for reagents pulling through?
Prahlad Singh
executiveYes. I mean, obviously, high content screening is a significant part of our platform business. It used to be around 25% or 1/4 of the business. And I think now it's about 1/3 of it. It's increased to about 1/3 of the business. High content screening, obviously, is critical as you look at drug candidates as to what the impact or what the effect it's having at the cellular level. And I think with the sensitivity that we bring to it, there is a significant amount of data, terabytes of data that are generated from it. And why it plays an important role now more specifically is with the advent of new technology, our high-content screening platforms would generate a lot of data. But basically, from a scientist perspective, they were only focused on looking at the kill, non-kill ratio essentially where the impact is having at the cellular level or not. But there's also a lot of incremental data, which they were not being able to leverage. Now with AI, they are able to leverage. And I think this is where we have started seeing a big funnel and pipeline coming Simultaneously, at the same time, a lot of companies are starting to build LLM models around these, right, trying to see as to how could we build models that would allow for faster screening of drug candidates. And this is where you are starting to -- we are starting to see more of a funnel and pipeline coming from nontraditional companies, right, companies that are, a, in the public domain generating data for LLM models, CROs and of course, the traditional pharma biotech customers.
Evan Stampler
analystHelpful. Like we said, I mean, you guys have been talking about AI since early part of this year. But even still, it did feel like there was sort of a sudden change in terms of that really inflecting and coming through on the P&L. So why do you think 2Q was kind of the moment that this idea actually turned into orders and revenues for you?
Prahlad Singh
executiveYes. I mean I appreciate that sort of the impact that was -- you were saying is sudden. But in our -- when we look at it through our lens, it was really pretty mapped out. I think, as I said, when we started talking about that this could potentially have an impact at the beginning of the year, there was some signs of it coming from our account managers and people in the field who were seeing more interest from traditional and nontraditional customers and inquiries coming in. In my -- if you go back and listen to my 1Q earnings call, we actually spent about 10, 15 minutes talking about as to how this could potentially play a role in drug discovery. And then when we came to the second quarter, we actually started seeing that in concrete evidence in terms of it translate those inquiries translating it into orders. And I think the resurgence was strong enough that these instruments, each one of them take about 10 to 12 weeks to make. So these are pretty complex instruments. So that's why you are sort of we saw more of a funnel which was big enough that we ended up with a stronger backlog than we have seen, I don't know, maybe even before COVID.
Evan Stampler
analystWhen we think about your broader portfolio, are there -- I mean we talk a lot about high-content screening, but are there other parts, maybe on the instrument side or elsewhere that we should be thinking about AI demand being a future driver?
Prahlad Singh
executiveYes. I mean we talk a lot about high-content screening, a, because of the sophistication of the instruments, and these are close to $1 million each, right? So they are big ticket items. But I think if you look at it from a drug discovery perspective, right, a researcher is looking at tissue, cell, in vivo, human cells, designs. So sort of our focus has been how do we build a platform portfolio and then back it up with the reagents that those platforms will need so that you have the razor-razor blade model going on. So you've got the high-content screening platform. You've got in vivo imaging, which still plays a very important role. And on the reagent side, we've got now a full suite of portfolio, which we will continue to build on similar to the acquisition that we did today that would allow us to sort of have the benefit of placing all these equipment today.
Evan Stampler
analystGot you. I mean just something came to me. Is there a reason that your high content screen, why is it open versus -- or would there be a benefit to having it so that like you have Illumina sequencer, you have to use this consumed -- I mean, is there a reason not to try to close it and have it be -- you have to use Revvity consumables and that's just -- or no. What is the thinking there?
Prahlad Singh
executiveI mean on the diagnostics side, it tends to be closed. We have closed systems simply because you have to go through the regulatory hurdle of getting approval on the whole workflow. Our belief is that we work with researchers hand-in-hand. As I've said this publicly, if you go to most labs, you will be -- you'll have a tough time differentiating who is a Revvity employee and who is a bench researcher from the institute. And then we don't want to encumber or force our customers to only use our reagents. We think that the merit of our instruments and our reagents stand by itself. And I think our goal is how do we build a workflow, full workflow that is convenient and easy for researchers to use. And then I think we -- both of them stand independently on the merit of their own basis.
Evan Stampler
analystOkay. Maybe going to A&G. I mean, I guess -- I mean, results there ex software, I think it was pretty similar to pharma biotech and I think up low single digits. I mean, is this -- how much of this was driven by like ex U.S.? How much of this was U.S. And kind of any interesting tidbits you might be able to add around the A&G market?
Prahlad Singh
executiveYes. I think the A&G market is still not what we would call back to fully normal. I think there is a level of stability there, but it's still not what we would consider it to be normal under circumstances. There is a level of uncertainty in academicians as to what the impact could potentially be or what else could come through. I would say it's a bit more stable in Europe than in the U.S., if I were to differentiate it by geography. I would say A&G is probably a bit more stable in Europe than the U.S.
Evan Stampler
analystHelpful. Maybe turning to software. Like you said, came in as expected, down 20% on a tough comp. up mid-single digits for the full year, which I think is kind of below -- I think you have been doing strong double digits the past couple of years. But the good news is the APV is low double digits. And so is that how we should be thinking about the business in the medium to longer term? Is this is a low double-digit growing business?
Prahlad Singh
executiveYes. I mean that's what we have it in our LRP, and it's done better than that. I think we have it at 9% to 11%, if I'm not wrong, in the LRP, and it's grown 12% to 13%. So it's done better than what we have said. I think given that the majority of our software business is still on-prem, you're going to continue to have these lumpiness quarter-by-quarter. But as you pointed out, Evan, if you look at the annual portfolio value, which is one way to look at what's the average revenue growth over a period, that business has done -- the APV has been double digits. Just to give an example, it grew 19% last year. And if you were to take 5% this year, it averages out to 12% over 2 years, which also happens to be the APV of the Signals business. But I think more importantly, if you look at our Signals business, 2026 is the launch of some of the most important NPIs in the history of that business. We launched BioDesign at the beginning of the year, Xynthetica. We are in the process of getting Signals AI out, and it's been just recently launched. And we've got LabGistics coming out, which is a key AI-based workflow. With these 4 key launches, I think the growth of the Signals business has just started. And then that's what I have said over the past couple of years. All the investment that we've made into the Signals business during the pandemic and from then on, is going to pay off now over the next few years with the launch of these key NPIs.
Evan Stampler
analystGot you. And maybe adding to that, I mean, these new products that you're introducing on the software side, I believe, are all SaaS only. And so as you -- can you kind of tell us where are we in the journey of going from on-prem to SaaS? And then with these new products, if I'm correct, being SaaS only, is kind of the goal? Or do you think this is ultimately like 100% SaaS? And kind of what's the trajectory to be getting there?
Prahlad Singh
executiveYes. I think we are somewhere between 32% to 34% SaaS right now. I mean, I think we will probably end up around 60 -- in the mid-60s in terms of what this business will be in SaaS. I think there will be always a component of our customers base for the signals business that will be on-prem, either for regulatory reasons or for in-country security reasons. So I think that's the assumption that I would make.
Evan Stampler
analystOkay. But is that true that all the new products are SaaS only?
Prahlad Singh
executiveAll the new products are SaaS. And then I think that also gives us an opportunity for incremental ways to look at revenue growth, whether it's through -- as AI comes into play, whether it's through computing or through storage, it just gives us incremental revenue opportunities as we look at it right?
Evan Stampler
analystImmunoDx, I think it just hasn't been getting a lot of attention because it's been doing so well. I mean I think high single digits has been growing. I mean is this -- LRP is 9% to 11% also, I believe. Is -- when -- I mean, do you think we can get to those -- the low double digits in this business? And what's kind of been helping drive the strength there?
Prahlad Singh
executiveYes. I mean I think, look, we are very happy with the immunodiagnostics business. And as I said, when we acquired this company in 2017, since then, as you pointed out, it's been humming along at a pretty good rate. I think the -- as I've said, the key for immunodiagnostics is autoimmune testing, in my view, is still in its nascency. I mean it's still not in mainstream clinical medicine. You still have to grow through several hoops before you are able to see an autoimmune specialist. And I think that will continue to drive growth, especially as you move from standard ANA screening to looking at specific disease areas around neurology or nephrology. There's a lot of undiscovered territory here, which is protected by IP, and that provides the opportunity for this -- the business to grow at what it has been growing. Ex China, it has grown in double digits. I think we are very happy with that growth. So I'm not sure I'm going to push that team to continue to do a lot more. If they can continue to keep the pace of 10% growth, I would be very happy.
Evan Stampler
analystGot you. I mean you said ex China. So what has China been doing in ImmunoDx? And then where -- when do we kind of lap those headwinds?
Prahlad Singh
executiveI mean I think it's -- right now, it's -- we are showing pro forma. Our revenues are pro forma anyway. So those are not accounted in our numbers. We expect that to close by the end of next year. And then I think that's when that business would be out.
Evan Stampler
analystGot you. Reproductive health, I think that business has been strong as well. I think you've been seeing very strong interim placements and you've had GEL. Maybe just maybe not just talking about GEL, but you did mid-teens in the first half, forecasting low to mid-single digits in the back half. Maybe talk about some of the puts and takes there.
Prahlad Singh
executiveYes. I mean just to be clear, we are forecasting low single digit in the back half. And it did well. Even ex GEL, I think reproductive health grew 10%. And that business has been -- again, I've been talking about that for the past decade. Reproductive health, specifically newborn screening has still a long way to go. There are still 100 million newborns that are not tested. So geographically, that provides us a lot of opportunity despite a declining birth rate. And there are a lot of rare diseases now, which are starting to see the advent of therapeutics coming out for them, right? Duchenne muscular dystrophy, spinal muscular atrophy and MPS II, these are starting to see therapeutics either get approval or being in the late stages of clinical trial. But identifying patients that would benefit from these diseases is still in its early stage. And that's where our newborn screening platform, which is fully ingrained across major geographies as a contiguous workflow that has a regulatory approval provides the distinct advantage by which it continues to grow.
Evan Stampler
analystGreat. Maybe on GEL, I think it set to expire middle of next year. Maybe just talk about maybe remind people exactly what you do there, how it's been going in England? And maybe how we should think about the continuation of that contract and when we might know about that.
Prahlad Singh
executiveYes. I mean, look, GEL is a great partnership with Genomics England, and they are a great partner and a pioneer in this area of doing population genomic screening, especially for newborns. And we've been very supportive of what U.K.'s initiatives have been since the COVID days. So we established satellite labs across the country during COVID and ran tests and that sort of eventually benefited us in continuing that partnership with Genomics England, for example, on population screening. I mean the partnership is going very well. We continue to do screening, and we will. And we are in discussions to see how we can prolong and then sort of extend this to adults or other avenues. I mean, obviously, this is -- the government is prerogative and they go through their regular process of doing tenders and getting approvals, et cetera, for budgets. And we remain hopeful that we will be there for the long term. But we've got other contracts and other partnerships with other countries and other institutes that we are continuing to explore. And in due time, we will -- those that are -- that allow us to publicly announce, we will announce those too.
Evan Stampler
analystOkay. Are there any of those -- would that be doing something similar to newborn screening or it be something...
Prahlad Singh
executiveIt's similar to what GEL is based -- it's like doing newborn whole genome sequencing.
Evan Stampler
analystRight. Okay. And have any of those discussions or anything been made public?
Prahlad Singh
executiveWe've got a lot of discussions going on, none that we have publicly announced yet.
Evan Stampler
analystOkay. Helpful. Okay. And then maybe just wrapping up on reproductive health. I mean, again, the mid-teens growth in the first half versus low single digit in the back half, what -- is GEL the main driver of that just as you lap that? Or are there other things that we should be?
Prahlad Singh
executiveWell, I think we had a strong -- I mean, as you pointed out earlier, with a strong instrument placement in the first half of the year and which we right now expect it to normalize. We expect it might do better than that, but that's what we have in our guidance.
Evan Stampler
analystOkay. Maybe on Life Sciences, I think you're looking for low single digits for the full year. I think you've talked about it kind of being a continuation of what you've been seeing, but there is kind of an uptick implied on that in the back half. So I assume part of this is software comps getting easier, but you also have some backlog in both instruments and reagents. So maybe just kind of unpack that for us and really what's driving that modest improvement in the back half.
Prahlad Singh
executiveSure. I mean I think as you point to software, you already pointed out, that's correct. It just sort of gets back to new contracts coming in and it's forecasted as such. I mean on the Life Sciences platform side, we expect that to grow mid-single digit in the third and the fourth quarter. Life Sciences reagents grew low single digits in the second quarter. We expect it to grow low single -- but in the third quarter, but better than what it did in the second quarter. And then I think we'll continue to see continuous improvement. I think the one way to think of it is that as you are getting these slug of platform instruments getting placed and go through their validation, sort of reagents tend to follow a couple of quarters later. So the more quickly we can install these equipments, get them validated, then the reagent flow through starts coming. So I think you will see that uptick continuing at a regular rate over the next couple of quarters. I think as I said, right, some of these instruments take 10 to 12 weeks each unit to be made. So you should sort of put that lag time in place.
Evan Stampler
analystI mean you did mention consumables taking some time to kind of flow through. Is there a way that you could frame the potential opportunity for -- I mean these are expensive machines. So I mean, how much do people typically spend on reagents or in a given year on these instruments?
Prahlad Singh
executiveYes. I mean it's tough to sort of quantify it because it depends on where it is, right? It could be in a university in some unique place versus it could be at a pharma biotech in New Jersey, which has got a very high throughput. So it's tough to sort of quantify the reagent pull-through that comes from these instruments.
Evan Stampler
analystOkay. I mean I assume if you're spending that much money on, I assume it's meaningful, right?
Prahlad Singh
executiveI mean that's the point, because if you're spending close to $1 million on the instrument, you're not going to mothball it and wrap it in plastic and keep it, right? The whole idea will be to have continuous throughput going through, especially with the advent of AI. I think that's the one piece that I think we -- and we'll continue to talk about this for a couple of more quarters till it sinks in. Because recall, as I said, first, a research scientists focus would be only on the region of interest that is this drug candidate having the impact on the cell that I wanted to -- that we were hoping to. And that was the area of interest they were looking at. But there is another now, especially with the launch of OptIQ, which we just launched, which has 4 cameras, right? There is -- there are terabytes of data now generated, which they can now take, combine it with the proteomic and the genomic data on that drug candidate and be able to extract as to the validity and activity of that drug candidate, which at a much faster pace, which they were not able to do prior to AI. So as that starts becoming mainstream, and this still -- again, mind you, this still is being done only in some institutes as this is taking place. Once this becomes mainstream, this is going to really take off.
Evan Stampler
analystNo. I mean it's interesting to say that. And so like I was going through my mind as you said that was I ask the question is, maybe you don't know exactly, but I mean in the past, were these instruments being constantly used? And if not, like it sounds like this opportunity enables that where you're just going to be constantly running these machines because you're finally actually able to -- you're going to be doing new experiments. You're not just going to be looking at one specific type of thing because you actually can analyze data now where you probably physically couldn't before.
Prahlad Singh
executiveI think the instruments were being used -- whether they were used constantly or not depending upon -- was dependent upon how busy the lab is, but not all the data that was being generated by the instruments were being used.
Evan Stampler
analystGot you.
Prahlad Singh
executiveI think it's more that, that data was not being used. But now with the ability of AI, you are able to take that, combine it with the proteomic and genomic data and be able to look at it in a much more wholesome manner much faster and get more productivity and efficiency out of the instrument.
Evan Stampler
analystOkay. So there's no reason to think that utilization/pull-through should go higher now. It was being run.
Prahlad Singh
executiveBut -- well, it depends, right? I mean not -- again, it depends on the lab the instrument, right? If I have a whole lot more samples than if I have only one instrument, -- the other benefit is.
Evan Stampler
analystSorry, now you have another instrument maybe. That's where it comes, yeah...
Prahlad Singh
executiveBecause remember, now you'll also have a whole lot more drug candidates coming because of in silico medicine, right? So this is actually going to end up being a validation bottleneck, which means that you'll, a, either have to get more real estate, place more instruments and do more screening because you have a lot more drug candidates. And this is where, if you recall, we started talking about this at the beginning of the year that we feel that screening of drug candidates will actually become a validation bottleneck. And to some extent, we are starting to see that, right, the early signs of that.
Evan Stampler
analystGreat. I think probably the biggest question we got, I guess, earlier this year on Revvity or one of the biggest was on the margin guide. And you guys had confidence in it. People questioned your ability. But now you've actually raised the guidance twice this year. Part of it is tariffs, but also just good execution. And I mean, I think it's -- I think the margins -- I think the guide still -- I mean you raised it, so I assume you have confidence in it, but there is still a tick up. And I think it goes to the low 30s in 4Q. I mean how should investors bridge that improvement into 4Q? And what's the potential for further margin expansion, I guess, because you will have a headwind from the tariffs. So I mean, how should we think about that going into next year?
Prahlad Singh
executiveYes. I mean, you raised a couple of very pertinent questions. I think of all the aspects of our business, I think the one where we have the greatest level of confidence is in our margin story because a lot of that is in our control, right? I mean just to the point, Evan, you said we've raised guidance twice, even if there was no tariff tailwind, we would still have raised our guidance on margin. And I think this is now with the tariffs, you get a 20%, 25% bps, obviously, tailwind. I think in the third quarter, all the cost initiatives that we have taken for starts bearing fruit, and we start seeing the impact of that in the third quarter. And in the fourth quarter, you will have your natural upsurge in volume that you see towards the end of the year. So I think we have a very high level of confidence in our margin story. And I'm just talking about what it is for 2026. Beyond that, if we start seeing the -- getting back to 4% to 5% organic growth. So if you take the 20%, 25% bps out, you're still -- baseline is still 28.5% and you get to 4% organic growth, you get another 50% margin improvement. And you get -- for our business, we get 40% incremental margin. So if we are in our LRP range of 6% to 8%, that gives you 75% operating margin improvement. So that's why I've said we have -- of all the things, we have the strongest confidence is in our margin story.
Evan Stampler
analystAll right. Great. One second left. So perfect timing. Thank you so much for coming, and it's great to see you, and thank you, everyone, for joining us.
Prahlad Singh
executiveThank you
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