Becton, Dickinson and Company (BDX) Earnings Call Transcript & Summary

September 16, 2020

New York Stock Exchange US Health Care Health Care Equipment and Supplies conference_presentation 27 min

Earnings Call Speaker Segments

David Lewis

analyst
#1

Well, good morning, everyone, and welcome to the Morgan Stanley Healthcare Conference 2020. As we enter day 3, we progress through the morning. It's my pleasure to have with us here, as we start here in the morning on day 3, Becton, Dickinson, and 2 members of management, both Tom Polen, CEO; and Chris Reidy, CFO. And then Kristen is hanging out there somewhere with a smiley face on the strip there.

David Lewis

analyst
#2

So we're going to dispense with my normal progression here. You guys have gotten used to these last 3 days talking about COVID upfront. I want to get with Tom's strategy here to start off our conversation. And Tom, I -- we've talked about this a little bit off-line, but I've covered the company almost 2 decades. It's dating myself a little bit there. I think investors have always appreciated the durability of Becton, Dickinson, the consistency of Becton, Dickinson. And I think in the last 6 to 8 quarters, they feel like they're seeing a different Becton, Dickinson. I guess the direct question to you is, is something structurally different about this business the last 6 to 8 quarters? Is this a different company post the Bard acquisition? Help us understand why that is or is not true and how this company gets back to the durable, consistent Becton, Dickinson they knew and loved from 20 years ago.

Thomas Polen

executive
#3

Yes. Sure, David. And thanks, obviously, for having us this morning. Great to see you, as always, and look forward to a good discussion here over the next 0.5 hour or so. But you've covered the company for a long time, obviously, and we've always appreciated your perspectives on BD. I'd say we do definitely believe it's more idiosyncratic in the past. And certainly, I'd step back. Of course, I'd been in this role now for about 7 months and took time coming into the role, looking at the exact question that you just asked as well. In the past, we have been impacted by some industry-wide headwinds like FX, drug-coated balloons and COVID. But we've also seen some company-specific matters. Alaris is a clear example of that. And so we are taking actions. I'm very focused on taking actions and making investments that strengthen our processes to both prevent and to better identify any potential matters that could arise in the future to get ahead of that. So -- and we're progressing very well on those.

David Lewis

analyst
#4

Okay. And the one message you've been trying to impart, I think, recently is ever since you took over in recent months is this business can get back to a 5% top line, double-digit or 10% bottom line growth profile. And maybe it's a question for you on revenue and a question for Chris on earnings. Why are you so confident? I mean a 5% and 10% business is a pretty good business. Why are you so confident in the 5%? And Chris, why are you so confident in the 10%?

Thomas Polen

executive
#5

Yes. So I mean number one is -- and I do have very high confidence in both of those goals. And what gives me confidence is not only our historical track record when you take out some of those items that we mentioned, but our strategy and how we're executing against that. And our strategy is built to deliver exactly that 5% and 10% in a durable way. And so first, right, we're very focused on driving that durable revenue growth of 5% plus. We've been reshaping our portfolio over the last couple of years. Bard is certainly a positive part of that. We're now -- our end markets are growing, excluding COVID times where all markets are, of course, at growth levels that they haven't been, some much higher, some a little bit lower, but getting back to a more equilibrium, I think we're seeing positive momentum in that direction. But our underlying markets are growing 4%, and we're investing our R&D dollars in markets that are growing even faster than that. Our R&D portfolio is in markets growing an average of 6%. And we're going to continue to drive our R&D portfolio in those directions. You may have heard we've recently started an innovation fund. Similar to what Bard had after the Gore royalty, we're utilizing some of the profits from Veritor and MAX COVID-related to start that fund ourselves. And of course, we also are in a position now to resume more of a normalized tuck-in M&A level, which will also help contribute to getting us into higher-growth markets and driving that revenue growth. Second, I'd say we're very focused on continued margin expansion, that 10%-plus adjusted EPS growth. We've talked a lot about our Project Recode, which is aimed to deliver $300 million in savings over the next 4 years. Our team hasn't missed a beat with COVID on Project Recode. We've been making the same investments that we planned pre-COVID, and we've been executing right to the schedule that we had pre-COVID. So we're feeling really good about how our team, which is largely operations, I mean, is doing well there. And then lastly, of course, we will continue to improve our balance sheet strength and flexibility going forward. And the May equity raise was a step towards that as well as the very active ongoing cash management programs that we've put in place.

David Lewis

analyst
#6

Okay. And this 5% to 10% profile, I know it's going to be somewhat -- the comps are going to be challenging here as you come out of COVID here. But this is -- as you think about 1 year forward, kind of fiscal '22, I mean, do you feel good about that 5% and 10% profile? And do you need to resolve Alaris before you can get back to a 5% and 10% profile? And how soon could investors see that underlying performance?

Thomas Polen

executive
#7

Yes, let me turn that to Chris.

Christopher Reidy

executive
#8

Yes. So you're absolutely right, we have to look at it on an underlying basis, and lots of things can happen in '22. We've been very clear that the lift that we get in Veritor in '21 is a variable in '22. So you have to -- we're going to give a lot of transparency to what goes up in '21 so that it would be very clear as to what happens in '22. So you have to normalize for that. You do obviously have the Alaris and how much that comes back. So we'll be very clear on what it looks like underlying. But we're very confident that on an underlying basis, we can drive that 5% plus and 10% plus. And I'd just add a few bits of color to what Tom said. On the Recode Project, we've done a good job of being able to deliver margin based on the synergies that we had coming out of CareFusion and the Bard deal. So we have improved margin. We have an infrastructure to do that. And Recode is really an acknowledgment that when you put 3 big companies together, you don't get all those synergies right out of the box. You get what you promised, but there's still a lot of complexity in the business that we can simplify. And that's what Recode is all about, and we can drive another $300 million of savings out over the next 4 years. So we're highly confident in the ability to drive those kind of margins.

David Lewis

analyst
#9

So you think underlying basis, Chris, you can get 50 bps a year out of this business, at least?

Christopher Reidy

executive
#10

Yes. And we've always been able to do that. I mean that's kind of a given. And then how do you drive more than that in a given year or over a period of time? And we've been able to do that, driven by simplifying, and that really was the synergies on getting that incremental dollar amount. And we think that there's still a lot of opportunity to do that. We've got the same people that went after the synergy savings going after the Recode savings. And so we're highly confident in the ability to do that.

David Lewis

analyst
#11

Right. And then, Tom, when you -- I think the fourth quarter guide, it seemed concerning to some, and I want to make sure that your trajectory is consistent with your peers. So on your procedure-oriented businesses, I thought your fourth quarter guide didn't really model a whole bunch of recovery. What we've heard at this conference so far is people in the procedure-driven world are seeing some kind of recovery. You kind of said the percent of number you saw in the third continues into the fourth. What are you seeing from a procedure-based recovery? And then, look, with these businesses like a BD and a Baxter where census and inventories and stocking matter, how confident are you that you have a good sense of the census for hospitals and sort of the inventory that's in the channel as we kind of exit the year here?

Thomas Polen

executive
#12

Yes. I'll turn it to Chris to make any further comments related to that. But maybe let me just make a comment that we feel really good about our execution and the performance that we have, very much in line with the guidance that we shared. And so I'll leave it at that. I don't know, Chris, if you have any other comment.

Christopher Reidy

executive
#13

Yes. I would just say that several months ago, in the absence of guidance, we did give some color on a monthly basis. And what we did say is that when we looked at June, we were in that kind of 75% of recovery on average. In July, we said that got up to 80% to 85%, and that's the color we gave. At this point, now that we've given guidance, we really want to kind of hold to that guidance and not go back to giving monthly updates on what we're seeing. But I think Tom's point that he just made there kind of tells you what you need to know, which is we feel very good about the progress of the business in the quarter. We're coming to the end of the quarter, and we feel good about the execution and the operations. And so that kind of tells you what you need to know.

David Lewis

analyst
#14

Okay. And then either for Tom or for Chris, I mean, one of the reasons I'm asking all these questions about sort of the structural business is, look, in recent months, you certainly have been trying to sort of control expectations for next year. Some of that is because of overzealous analysts, maybe myself included, on Veritor. But the real question is heading into next year, it's fine to control expectations. And given what the company went through the last 6 quarters, I frankly want to control expectations. But I want the investors to appreciate that there's nothing structurally that's sort of gone wrong here. So maybe just help us understand, there are some dynamics of MMS and MDS that create some bad comparables. Other than these comparable dynamics, has anything changed in the last 60 days? Or this is just making sure people have idiosyncratic financial points about fiscal -- the forward fiscal year?

Thomas Polen

executive
#15

David, I like the fact that you said you'd be doing the same thing. And there is no -- to your point, nothing has changed in that period of time. But a couple of things. Let me just start off by saying, first off, we recognize there's a need and an opportunity to better communicate with the investment community. And you've seen us make investments and bring in talent to do exactly that. And so to that end, right, last week, we publicly made some comments in the spirit of exactly that, better communicating, engaging with the investor community. And so as I also said, we continue to be very comfortable on the progression of our strategy and also how operations are performing in Q4. For '21, right, we haven't provided any guidance. Obviously, November will be here before we know it, and we're not going to comment specifically on '21 before then. But we also thought it's going to be helpful because it is a very complex time in the industry with what's going on with COVID. Obviously, with some of our new innovations that are COVID-related, they add another level of complexity. They're great opportunities, but how do you model them? And of course, you've got their pump business as well. And so all these complexities, we recognize the need to give some clarity to help people in their modeling, and we made a couple of observations. And maybe let me just reiterate some of those right now just to be helpful. Again, we said, first off, there's a wide range of Veritor estimates, some in the $1.5 billion to $2 billion range. Some of them seem to -- those seemed aggressive to us given variables around vaccine timing, supply and demand and ASPs, and then it would be more prudent to take a more conservative view on that. And if it ends up being in that range, that's something that can be increased through the year rather than assume that, that were to evolve that way. We don't think that would be prudent. The second thing that I made the comment is, is that related to those new innovations on Veritor and MAX, I commented on this earlier, that we're going to be reinvesting a portion, an appropriate portion of those profits back into the business to drive our strategy of durable, long-term growth. And we talked about the innovation fund. We haven't quantified how much we'll be reinvesting at this point in time. Part of that will wait to evolve depending on how those products evolve, but we'll be prudent. We're not going to invest ahead of the curve on those. And then we reminded also for those that aren't as familiar with the stock that we're one of the very few companies who have a September year-end. We still face a tough COVID comparison in the first half. We actually don't annualize until Q3 the COVID impact. And so again, we thought it was more prudent to assume that we don't get back to pre-COVID levels through '21, that there can be some underlying pressure on health care. We just made those comments, specifically called out MDS as the area that some of the Street models seemed a little aggressive. We expect a more modest growth in MDS specifically that was impacted as -- based on what we are seeing. And then we also pointed out that in infusion pumps, we had difficult comps because Q1 was a full -- a partial quarter before the ship hold. And then, of course, we had an abnormally large bolus of sales in Q3 due to the huge demand from COVID in both the U.S. and in Europe. And so Chris, I don't know if I've missed anything you'd like to add.

Christopher Reidy

executive
#16

No, I would just add 2 things. One is just more housekeeping that when people update their models, they should adjust the base in '21 going through to '22. So that's one housekeeping. But more substantively, I think the comment that we're making around the first half of the year being a tough compare for us to pre-COVID levels and the fact that we don't think it's prudent to assume that you get back to 100% of pre-COVID levels immediately, the combination of those things really also have an impact on gross margins. So what we would think is that the first half year is going to have a decremental margin impact. And we gave a lot of clarity on that in the third quarter and the fourth quarter. And what we said was that the decrement in the third quarter, which was the peak period where the revenues were impacted, we said it would be about 80% flow-through, and that was about 390 basis point drag. As you move forward to the fourth quarter, we said it would be about half that. Now you would expect it to improve in the first quarter and the second quarter, but it's still a drag on margins. So we just want to make sure people understand that and have that in their models as well.

David Lewis

analyst
#17

And Chris, just getting to this notion, making sure there's nothing fundamentally wrong, I want to push you a little bit on some of these fund numbers. I mean Street consensus numbers were kind of $12 to $14. So maybe the $14 number was a little goofy. But the Street consensus really was more like $12.75, and yet you still seem a little uncomfortable with that number heading into next year. And I appreciate you're trying to control expectations. But if I just say, look, the core business does low-single digits, like 3-ish kind of percent next year and gross margins get back to kind of 56%, that kind of gets me to kind of like $11.70 kind of number. When I throw in $1 billion of Veritor, I can still get back into the low 13s. So to be pushing people closer to a $12.50 number, either, a, I've got to be wrong about the core; or b, you're really going to invest a lot of that Veritor savings. And remember, $200 million is 1 point of R&D. That would be 40% of the Veritor money, which is that's a lot of money. But just help me understand, I mean, $11.70 in the core, plus $1.25, $1.50 in Veritor...

Christopher Reidy

executive
#18

I appreciate you trying to get us to comment on consensus, and it's too early for that. When you think about the dynamics of the market right now and how difficult it is to predict, we don't want to get into that level of specificity. And there's time for that. We'll certainly be talking about that in the future. And I think what we're trying to do is not to guide to a specific number, but just make sure that people have color on specific observations that as we look at it, there's a number of analysts that do seem to be getting too far in front of themselves on Veritor, for example, and we've addressed that. We think that, in general, people are forgetting that we're going to have a half year difficulty compare for MDS. And we haven't gone into too much detail on MMS. But again, we had a bolus in 2020 from MMS, from medical necessity as well as the first quarter of pre ship hold, and that's going to be a tough compare next year. So we want to get that out there. So we haven't really addressed specific models yet. And I understand the interest in wanting to do that, but I think it's too early for that. But we did want to give that level of color. And I think the point that I'm making additionally today is that margins, we really got to look at the margins in terms of that decrement as you look through. And then, of course, there are -- assuming margins that are a little richer than we would expect.

David Lewis

analyst
#19

And Chris, if you're going to give us an annual guide, are you going to give us an annual guide for the corporation and guide more quarterly on Veritor? Are you going to give us an annual Veritor number?

Christopher Reidy

executive
#20

We actually haven't made that decision, David. We're giving color, but we're not committed to giving an annual guide. I think that the market is so dynamic right now and we gave guidance for the fourth quarter because we felt like we had the visibility in that near term. We have to make that decision as we approach November as to how we feel, and we truly haven't made -- given ourselves the opportunity to react to what's going into the market. So we haven't made that ultimate decision. We'll see what happens as we get closer to November.

David Lewis

analyst
#21

Okay. And Tom, just 2 more things I want to cover to you before we close out here in the next few minutes. What is just obviously Veritor, right? Like it or not, the most important catalyst in the business right here. You're wanting to kind of rein people in and control expectations for next year. You've talked about it being vaccine-driven, ASP-driven. How much of this is tied to just the proliferation of sort of lower-cost, higher-volume antigen test?

Thomas Polen

executive
#22

It's not tied to that at all. I think it's just recognizing a number of uncertainties related to vaccination campaigns, related to the prevalence and the persistence of a pathogen that spontaneously showed up and will eventually go away, whether or not that's from a vaccine or whatever other means under -- that control it. We just don't think it's overly appropriate to speculate that on a -- one end of the extreme is take a more balanced approach on it. I'd say as you think about the varying different new entrants into the space, first off, there's a big need for additional testing. So we certainly welcome and are happy to see additional products come into the marketplace. We continue to have extremely strong demand on Veritor. It's around production, is the limiting factor. It's not demand at all. Demand certainly still exceeds supply, not only for us, but I think for the industry as well. I've talked before that certainly, our ramp versus the expectations that we had shared, 10 million in the first quarter, getting to a run rate of 8 million a month afterwards is very much on track, if not slightly ahead of our expectations, as you can expect from us. And I've shared in the past, manufacturing is a very strong core competence of ours. And so we feel really good about how we're ramping up production to those numbers. And again, perhaps in Q4, we'll run slightly ahead of some of those. So performance of the test, we also feel very good about. And of course, there is a difference between those manually read tests, which, of course, we used to sell those as well. We purposely invented and others invented that next-generation technology of instrumented read platforms, which come with their own performance benefits. And we feel very confident in that. They always have maintained a price premium. Because of those performance benefits versus manually read tests, as you look at -- actually, they won the game when it came to other respiratory pathogen testing like flu, it's almost all instrument read because of the performance. And so they certainly both have a place today. There's just an overwhelming need for more rapid COVID testing, but we're also very comfortable in the position of instrumented higher level platforms as well.

David Lewis

analyst
#23

Okay. So you don't -- you think you can still price the value. You don't feel inclined to have to lower your ASP because we have $5 card-based testing?

Thomas Polen

executive
#24

I don't want to say that we see $20 ASP through the year. I don't know the -- we don't see that changing right now. Q4, we're right in line with that. And we don't feel pressure to change that at this point and nor would I ever see us getting pressure to move all the way down to that level. There will always be a strong premium for instrumented-based platforms. So my only point is if you were to ask exactly where the price is going to be in a market that just was created in the last 60 days and where it will be 13 months from now, I can't tell you with certainty. I don't think anyone could tell you with certainty where exactly that's going to be to the dollar. And of course, when you're marketing -- when you're selling tens of millions of tests, those numbers matter a lot to the dollar, which, right, $1 difference here and there adds up to a lot of money. And so that's why -- and again, that's in the spirit of prudence. It's nothing more than let's just be prudent. Does it -- where does it evolve to by the end of the year? But we certainly wouldn't see it going anywhere near those single-digit dollar numbers.

David Lewis

analyst
#25

Okay. And look, obviously, with every antigen test and every sort of non-laboratory-based PCR test, every platform has had some criticisms around test performance, and you were no stranger in this last couple of days. You've put a statement out with this, but I'm assuming you are very comfortable with your testing, kind of the veracity, sensitivity and specificity of the testing?

Thomas Polen

executive
#26

Yes. Well, we are. And of course, you've seen some recent data that we published last week that just reinforced the performance of Veritor, as we expected. And just to give a little bit of color because, obviously, there was some reports from nursing homes. Very small number of nursing homes, of course, did report false positive results. A small percentage of false positive results are not expected with any antigen tests. You can see that, right? We have 100% specificity with a confidence interval -- 95% confidence interval puts you at an expected specificity for anyone with 100% claim of 98% to 100%. So you're expected to get -- could have some. And so we're doing, as we always would do, that we take every complaint seriously and that we have an investigation underway. Well, look, there's specifically -- where we saw some clusters, we're also looking at training and other things there within what is a brand-new user base of this technology. To keep in perspective, we just shipped out 11,000 Veritor instruments to nursing homes around the country who all now just started to use them simultaneously. And so we're getting really good feedback. We have a telesales team that engages directly with those nursing homes, and we get a lot of really positive feedback. Again, we've got a small number of nursing homes who have reported a higher rate of false positives, and we're working with them to investigate the root cause. But overall, again, we feel good about the performance of Veritor and the assay itself. We're not seeing those same rates at all in our -- we're not getting reports within the traditional hospital laboratory customer base either. It's just a separate data point.

David Lewis

analyst
#27

Okay. And a little bit time to get that one and make sure we touched on Alaris, which is probably the other major catalyst for the story the next 6 months or so. And as I see it, I'm just oversimplifying this on Alaris, there are 2 dynamics. One, you have to convince the FDA that the product in the field is similar to the file on file with the FDA. And you got to convince them that the product is safe. So 2 questions to you. But how confident are you that this product is safe and this is not a question of safety? And how are you feeling about the deliverables as it relates to the semantics around the file that you have to update now versus you did 6 months ago?

Thomas Polen

executive
#28

Yes. First off, my confidence in the safety of Alaris is extremely high. So let's just make that very clear. And I've always said that from day 1, I think certainly the fact that our customers also feel that. And the FDA is supporting us, continuing to ship Alaris out. We shipped to more than 1,000 customers during the COVID pandemic to support expanding their fleets to help them deliver very high-quality patient care. It's not by accident that we have 70% market share in infusion pumps, and that's because of the unique advantage and benefits of the product. With that said, the product is different than what was on the original file. It's improved over the last more than decade, right, before we owned it. And there were improvements made that, as we've said, should have had updates to the file on those improvements, and that's why we're submitting an updated 510(k). That's the root of the issue. But we have very, very high confidence in the safety of the product. So of course, my highest priority, the highest priority of my leadership team is getting in that 510(k), and remediating the situation. We've always said as part of that priority, if we have to choose between rushing in and getting a submission done versus getting the right submission in, we're going to choose the right submission, the highest-quality submission because our goal isn't to get just the submission, and it's to get the 510(k), the updated 510(k) approval. And the best way that we do that is giving the FDA all the information they need the first time, working collaboratively with the FDA to understand all the questions that they may have ahead of submitting that, making sure that we answer their questions through the testing that we provide them ahead of the submission. And we're really pleased with how collaborative -- the FDA and us are working very collaboratively together on this, very supportive. We've been getting very active feedback. We've been incorporating that in our testing protocols. Of course, we gave an updated time line on that submission. And we feel good overall about the continued progress towards those exact milestones and dates that we had shared.

David Lewis

analyst
#29

A more fulsome submission, the hope would be it would lead to some type of expedited approval. My sense is we can get this in the second or third quarter of fiscal year, this could be approved within 6 months or so or less from that submission. So your confidence level that this can be approved by the end of the next fiscal year?

Thomas Polen

executive
#30

Yes. I don't want to speculate on time line for approval. Again, what I can -- what our team controls is getting the best high-quality submission into the FDA within the time lines that I've shared. And once it leaves our hands to the hands of the FDA, and that specific time line will be under their control. Of course, the easier we make it and the more complete data package and the better written that is, the faster that time line will be. But I don't want to speculate on that. Keep in mind, this is a large 510(k) submission. Pump submissions are probably among the more complex 510(k)s or if not the most complex 510(k) submission that one can make. But setting that aside, we're focused on making sure it's the right submission, to make that as expedited of a process as possible.

David Lewis

analyst
#31

And you still feel good about the 2Q, 3Q timing you provided for the submission?

Thomas Polen

executive
#32

Yes, absolutely.

David Lewis

analyst
#33

With that, we're 2 minutes over, team. Tom and Chris, thanks so much for being here with us this morning, and enjoy your day meeting. I appreciate you joining the conference.

Thomas Polen

executive
#34

Okay. Good seeing you, as always, David. Thank you. Thanks, everyone.

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