Ladies and Gentlemen, good day and welcome to the Piramal Pharma Limited Q1 FY 2026 Earnings Conference Call. As a reminder, all participant lines will be in the listen only mode and there will be an opportunity for you to ask questions after the presentation concludes. Should you need assistance during the call, please signal an operator by pressing star then zero on your touch-tone phone. I now hand the conference over to Mr. Gagan Borana. Thank you. And over to you sir.
Thank you, Rio. Good morning everyone. I welcome you all to our post results earnings conference call to discuss our Q1 FY2026 results. Our results material have been uploaded on our website and you may like to download them and refer during the discussion. The discussion today may include some forward-looking statements and these must be viewed in conjunction with the risks that our business faces. On the call today we have with us our Chairperson Ms. Nandini Piramal, our CEO of Global Pharma, Mr. Peter DeYoung, and our CFO Mr. Vivek Valsaraj. With that, I would like to hand over the call to Ms. Nandini Piramal to share her thoughts.
Good day everyone and thank you for joining us today for our post results earnings call. The quarter was broadly in line with the guidance we shared for FY 2026 in our last quarterly call in the month of May. While there may be some lumpiness in our sales between the quarters due to the nature of the CDMO contracts and timing of institutional orders in the CHG business, we believe we're largely on track for meeting our full year FY 2026 guidance of mid single digit revenue growth with mid teen EBITDA margin and YoY growth in net profits. During the quarter, we reported a YoY revenue decline, a djusting for the impact of destocking in one of our large on-patent commercial CDMO products, the YoY revenue growth was in early double digit.
Our CDMO business base business, adjusting for inventory destocking, delivered mid teen revenue growth during the quarter accompanied by improvement in EBITDA margins mainly driven by our overseas sites. In our CHG business, while we reported a muted growth in Q1, we expect growth rate to pick up significantly, more specifically in H2, given the timing of shipments and phasing of institutional orders. Our consumer business delivered a healthy growth of 15% during the quarter driven by healthy growth in our Power Brands and e-commerce sales. Lower interest costs due to reduction in interest rates and lower effective tax rate helped us deliver 8% YoY growth in our net profits for the quarter. On quality and compliance, we successfully maintained our best in class track record of zero OAIs since 2011. This quarter, we successfully closed the U.S. FDA inspections at our Aurora facility and in Canada without any observations.
We also got the U.S. FDA approval for our Digwal facility at Sevoflurane API and finished product manufacturing site for both human and veterinary use. On the sustainability front, we continue to make steady progress in multiple areas including water and waste management, afforestation, renewable energy adoption, diversity, inclusion, human rights, and occupational health and safety. These initiatives are beginning to show tangible results and reflecting meaningful improvements in our ESG scores by external agencies. Moving on to business specific highlights, starting with our CDMO business. O ur CDMO business reported a revenue around INR 997 crore, which was a YoY decline of 6%. However, adjusting for the impact of inventory destocking, one of the large on-patent commercial manufacturing products, the business delivered mid teen growth. The growth was primarily led by our overseas facilities, coupled with a YoY improvement in profitability.
Our nutritional supplement business and generic API business also delivered encouraging growth during the quarter. On the profitability front, we continue our efforts toward cost optimization through better procurement strategies and operational excellence initiatives. This, along with the scaling up of our overseas revenues, should help generate operating leverage to help improve our EBITDA margin toward 25% by FY 2030. In terms of order inflows, we've had a mixed experience during the quarter, with some of the overseas sites experiencing good order inflows, whereas the early stage discovery and development orders continue to see slow pickup due to an inconsistent and incomplete recovery of biotech funding, coupled with geopolitical issues and uncertainty over trade policies. During the quarter, we broke ground in our capacity expansion project at the sterile fill-finish facility in Lexington, U.S., which is expected to be completed by 2027.
This expansion should lend impetus to an integrated ADC development and manufacturing program over the medium to long term. Moving to our Complex Hospital Generics. Complex Hospital Generic during the start of the quarter, we commercialized new Sevoflurane manufacturing lines at our Digwal facility to complement the existing Sevoflurane manufacturing at our Bethlehem facility in the U.S. These new Sevoflurane manufacturing lines at our Digwal facility should be catering to the emerging markets as well as the U.S.. We have already started seeing a good pickup in our inhalation anesthesia sales in some of the emerging markets and expect this momentum to continue going forward as well. We did see some slower revenue booking in our key markets in Q1. That's largely due to phasing that's more skewed to the later part of the year.
I n Injectable Anesthesia and Pain M anagement segment, o ur strategic initiatives aimed at mitigating supply limitations are advancing as scheduled, with benefits expected from FY 2027 onward. On the specialty and differentiated portfolio front, during the quarter, we launched Neoatricon in select EU markets. We expect to launch in more markets during the rest of the year. The initial response has been good. Moving on to our Consumer Healthcare business. Ou r PCH business delivered a healthy growth of 15% during the quarter. This was primarily led by an 18% growth in our Power Brands and a 41% growth in our e-commerce business. We launched seven new products and SKUs during the quarter. We continue to invest in media and trade spends to boost the growth of our Power Brands along with improvement in profitability metrics. Our Power Brands grew 18% during the quarter and contributed 49% of the total Consumer Healthcare sales.
Brands such as Little's CIR and i-range were amongst the key drivers of growth. The i-range experienced muted growth last year following the regulatory price control on i-Pill. With this impact already in the base, it is witnessing a healthy recovery in the current financial year. Our sales and e-commerce platforms continue to demonstrate strong traction, coupled with an improvement in profitability. It grew 41% during the quarter, contributing to 23% of PCH sales versus 19% in quarter one FY 2025. Summarizing the quarter, CDMO business excluding the impact of destocking delivered good mid-teen growth with YoY improvement in our EBITDA margin, primarily led by better performance in our overseas sites. Our CHG business is also tracking well with healthy demand in analgesia and anesthesia, complemented by on-time capacity expansion. This should start reflecting in coming quarters, especially H2, given the timing of shipments and the phasing of institutional orders.
Our consumer business continues to grow in line with our expectations, led by the Power Brands and e-commerce sales. We remain on track to deliver FY 2026 and FY 2027 guidance that further meet our FY 2030 aspiration to become a $2 billion revenue company with a 25% EBITDA margin with h igh teen growth. With this, I'd like to open the floor for Q&A .
Thank you very much. We will now begin the question and answer session. Anyone who wishes to ask questions may press star and one on their touch-tone telephone. If you wish to remove yourself from. the question queue, you may press star and two. Participants are requested to use handsets while asking questions. Ladies and gentlemen, we will wait for a moment while the question queue assembles. To ask question, please press star and one. First question i s from Amey Chalke from JM Financial. Please go ahead.
Yeah, thank you so much for giving me the opportunity. First question I have is on the CDMO order book. How is it looking for FY 2026? Is there any change over last quarter in CDMO order book and i f you can quantify?
There's been no material change in the order booking since we spoke last quarter when we gave the guidance for the year. The first quarter we have had order booking that has progressed within the quarter. There's been no notable uptick versus where we were at or expecting at the beginning of the quarter, nor no notable downtick. It's been consistently performing, but at a modest level, as described by Nandini in her comments. The situation with respect to our clients' ability to raise money, and once raised to spend money, remains where it has been mostly since the middle of January.
Sure. The second question I have, are there any project wins during the quarter which you like to highlight, or you can give some color on if there are any new launches which would happen during t he year or maybe over two years?
We appreciate the detailed question. We would like to reaffirm that the outlook for the year remains the outlook for the year and that the revenue growth outside the destocking event is in the mid teens, which we described, and the order booking is consistent with that expectation. We don't typically give specific customer order booking comments because first, our customers ask us not to communicate that level of information, and second, we think that ups and downs of individual customers in the ordinary course don't particularly give useful information, and we suggest you look at the aggregate numbers we've given for the full year guidance.
Sure. The last question I have on the margin front, despite the flattish growth f or l ast quarter, margins have dropped a bit. Does that mean that our core business margins have come down?
Amey, if you refer back to the annual guidance that we gave, we did indicate that there will be some moderation in margin given the fact that we will be growing in mid single digits. It's largely the impact of the destocking of the order in the CDMO space which is leading to some moderation in the margin, and this is in line with what we had guided for.
Sure, sure. Thank you so much. I will rejoin .
Thank you. Next question is from Abdulk ader Puranwala from ICICI Securities. Please go ahead.
Yeah, hi. Thank you for the opportunity. My first question is with regards to the impact of this large innovative product. Could you help us understand that, you know, is there any particular quarter where the sales of this product would be higher during the last year or it was, you know, kind of evenly spread? The reason why I ask you is that your quarterly numbers kind of fluctuate every time. Any color on the slumpiness along with some indication on the last product would be fruitful.
I'll comment and Vivek can add in anything further. The first is that last year we had the benefit of that large product reasonably evenly spread throughout the year. This year, as we guided when we laid out our expectations for the year ahead, which we're currently in, we do n ot get that benefit.
I think the only additional point I would mention is that Q1 for us in the fiscal year is typically a softer quarter. When you take away a large profitable base business across all months in a traditionally soft quarter, you can see a more profound impact on operating leverage, which would be showing up in the numbers.
To reiterate, Abdul, that H2 continues to be bigger than H1 for us as it has been in the past, probably more prominently this year given the fact that even the CHG business, we did see some slowdown in quarter one, but we do expect the growth to recover more specifically in H2.
Understood, sir. My next question is with regards to your investment in ADCs. I understand you're investing $19 million at your Lexington and Riverview facility, but in terms of the revenue trajectory or the order outflow to happen, when exactly do you see this opportunity kind of playing out for you?
The ADC opportunity is the largest contributor to the revenue, and that is our conjugation facility in Grangemouth, U.K. It is supported through the Lexington fill/finish, the Riverview linker payload, and the Hyderabad/ Yapan map. From an overall growth projected, this is a rapidly growing business for us and it's contributing a lot to what we show in our, i t's one of the big contributors of what we call the differentiated offerings bucket. If you look at our full package we shared with our annual report, you can see the multi-year trend in differentiated products is a demonstration of growth. Now, just one clarification. The expansion that we announced at Lexington and at Riverview, the linker payload at Riverview is entirely and only dedicated to ADCs. However, the expansion at Lexington has multiple benefits.
The first is its onshore containment-oriented fill/finish for any purpose, and we see significant and strong demand for that. The second is its onshore capacity in an environment where people are looking for U.S.-based production for drug product, and we are benefiting from that. The third is exactly what you mentioned, which is the linkages with ADCs in an integrated offering, which we will also benefit from. We actually see three reasons behind the overall growth in terms of the Lexington facility, and ADC is only, let's say, one of those three in that example. We're expecting and should see growth in the Lexington business for that purpose. I just want to reiterate another point that was covered in Nandini's comments, which is a lot of our growth so far this year has been in our overseas facilities.
Fair enough, thanks for that detailed explanation. Peter, to understand, when we are calling out our 2030 guidance of achieving close to $2 billion of revenue, is ADC also factored into that guidance?
Absolutely. If you want a longer answer, we can give it, but the short answer is yes.
Understood, sir. Just lastly on the margin outlook. W e are maintaining the low teen margin guidance, what we have given previously.
Yes, we're sticking by FY 2026 guidance and we're on track for that.
Got it. Thank you.
Thank you. Next question is from Shyam Srinivasan from Goldman Sachs. Please go ahead.
Good morning. Thank you for taking my question. Just on the commentary around the overseas sites, if you could help us quantify or give some direct qualitative sense on the utilization improvement, which of the sites where we have seen additional demand come through. Just some qualitative color or even quantitative color on those overseas sites, please.
What's nice is that we've seen strength in our U.K. sites, both of them in terms of, I guess you could call revenue as a proxy for utilization, and also in a significant number of our North American sites. What's nice is that it's not a single site and it's not a single country. It's actually across three countries. We're seeing the growth, Canada, the U.S., and the U.K., and it's across a number of our overseas sites. It's nice to see this year. Obviously, we have some of the challenges we described earlier, but it's nice to see some growth in our overseas offerings as demonstrated through revenue.
Okay. I s this, Peter, the biggest driver for the CDMO margins improving, like ex of whatever the destocking? Is that the key driver of improvement in margins?
Yes.
Yes. The balance growth, I think again helps us overall.
To give further color, we've described the tremendous benefits or detriments of higher or lower revenue in our overseas sites, many of which are on the smaller side, and the operating leverage impact is significant. When we have these improvements, that helps. The second one you may notice is the EBITDA to PAT conversion ratio. When we get this benefit, we also, because of past actions, do not have a lot of tax outflow. This is another positive when we see this go in this direction.
Okay, thank you. Second question. Just trying to decode the mid teen growth in the CDMO business excluding the one-off, r ight? Did we have any sales of this number one product for us in the quarter, or was it nothing?
We did not expect, anticipate, or communicate an expectation around any sales in the quarter, and we did not have any.
Okay, we can say base had that number and nothing this quarter. When I do a simple math of assuming 15%, that product comes to close to 20% of your CDMO revenues, is that how we should look at it?
We would avoid getting into specific product related revenues here, Shyam. Yeah, you're doing your math. We would avoid speaking about specific revenue contribution.
Got it. My last follow up on this one is, you know, anything, I know you. These are lumpy and we don't, and we have guided for fiscal 2026. Is there any early indications, Peter and team, to see that this product should come back 2027? There are some competitors as well which are, you know, we can see through export data. Some of them are shipping it. If you could help us understand the landscape. I don't want a quantitative number from you, more from a qualitative or a comfort that this product probably comes back.
We don't give specific level guidance, and our customers request us not to do that. I would just give one qualitative comment, which is we remain the primary supplier for the U.S. market, and we expect that when the destocking has completed, orders will resume. It remains the choice of our customer, not ourselves, and we look forward to their future decisions.
Thank you. Last question is on the CHG business. The growth starting from quarter two which you have telegraphed, what is driving it? Is it more emerging market? Has there been any issues in our U.S. market in terms of market shares or something that has also led to slowdown this quarter, which could c orrect. Any directions here on CHG? Thank you.
We would anticipate a lot of the growth coming from the existing inhalation, injectable pain, and intrathecal business franchises. We do have some additional sales expected in the second half, and we would see a meaningful part of that being in our ex U.S. markets for the growth. As we look at the difference between, say, last year and this year, that does not change from what we communicated when we discussed the guidance for the full year. It's just that it's not all happening in the beginning, it will happen more back ended.
Thank you. Thank you, Peter.
Thank you. Next question is from Maitri Sheth from Choice Institutional Equities. Please go ahead.
Hi. Thank you for the opportunity. Just one question on the gross margin side. Our gross margins have largely remained in the 62%- 64% range, 65% range f or the last two, three years. Can we expect to see some improvement there, i f you could quantify that?
At the current levels, gross margins are expected to remain in the range of 64%- 65%. As the quantum of on-patent commercial products and our innovation goes up, we do expect some improvement in the years ahead. At this stage in the midterm, it would remain at the same.
Okay, that's it. Thank you.
Thank you. Before we take the next question, a reminder to participants that you may press star and one to join the question queue. The next question is from Matangi from Motilal Oswal. Please go ahead.
Hi, am I audible?
Yes, yes, go ahead.
I understand that there are many new SKUs that have been launched. I'd just like to understand what are the breakeven timelines for this and if we expect any execution risks.
Is this for the PCH business, the Consumer Healthcare business?
Oh yes, all of them, across.
No. The SKUs were launched in the Consumer Healthcare business. The business itself is actually making an EBITDA profit. That is what we continue to expect, that we will improve profitability as we get to scale. I can't give you on a brand by brand or SKU level, break even. The business as a whole is EBITDA profitable.
Understood. Okay. My next question is about the customer concentration risk here. Are we taking any steps to reduce customer concentration in the CDMO segment or do we not expect this restocking issue to resurface?
I'll give you two parts to this. The first is that in the innovator CDMO business, when new launches happen, and I think we discussed this when we did communicate the guidance last year, a typical move after a launch happens from an innovator customer is to evaluate stock position versus the amount of inventory they bought for the best case scenario. You do see, from time to time in the U.S. and our competitors, these events do happen. With any given new launch, you can expect at some point in time there could be such an event. This one was more pronounced because it was our largest customer product relationship and obviously had a big impact as a group. We decided when the orders came to take them because it was better to have them than to not have them.
We also identified in our risk committee, for obvious reasons, as you described, that there is customer concentration risk. There are significant efforts underway before and also now to add new business to the site and to the business so that we can reduce that reliance. That's part of what's driving, with Nandini's comments, the 15% growth that we're seeing across all of the business aside from this specific customer product combination. Yes, we recognize the risk. Yes, we took the business and yes, we're taking efforts and seeing some benefits from, but not yet enough of our efforts to diversify.
Understood. I just have one last question. I understand that operations are quite dependent on the U.S. FDA inspections. I'd like to know if you expect any new trade and regulatory policies and tariff risks in the U.S..
I think we've maintained a successful OAI status since 2011. I think we're pretty confident of quality standards and audit facing inspections. However, I think on trade and tariffs, there is uncertainty and I. Wouldn't want to comment on that.
Understood. Thank you so much.
Thank you. The next question is from Madhav, from Fidelity. Please go ahead.
Hi, good morning. Thank you so much for your time. Just wanted to understand that for the large on-patent commercial product supply, which is going through destocking, how is that product doing in the end market? Does it continue to grow in the double digits for the end market sales for that product? If you could share some color so we can have a sense in terms of the ability of our supplies to recover once the destocking is over.
I would encourage you to look at equity analyst coverage of that company or public filings from that company, both of which could answer your question, or even newspaper articles about that company, all of which would show it's a growing product.
Yes. That actually indicates it's growing at 15%- 20%. I just wanted to confirm with you that once the destocking is over, this should come back for us in a good way, r ight? I mean, that's what.
I would encourage you to do another pass at that. You may see a higher number. Even some of the analysts on this call, their firms cover this so you can pull it down. I think it would be better than that number. I would suggest you look at your own primary sources.
Okay. Okay. How is the conversation with this client? How much time do they expect the supplies to come back? Is it something which is more? Wait and watch at this point?
We talk to them nearly every day, and we will await their decision once the stocking levels have come down to their target level.
Understood, understood. Just a second question on the CHG business. I think we had added a fair bit of capacity and we were quite sort of positive on scale up here. Should we take the softer growth in Q1 more as just like you flagged some timing of shipment issues, et cetera? On a full year basis, can this business grow in the double digits for us?
Yes, I think we stand by our guidance overall. As with the CHG business, achieving, you know, it's sort of linearly, it's on track for achieving the FY 2030 goals. Yes.
No, I understand, but I'm saying that can the CHG business, with all the new capacity in the ex U.S. markets we're targeting, can it grow in double digits this year despite the soft Q1?
Yes.
Okay.
If you remember last year we did a stronger Q1 than what some of you all thought we would do when you asked us if we would raise the guidance. We encourage you to look at the full year numbers. This year we have it in the other direction and we again encourage you to look at our full year numbers.
No, I understand that. Thank you.
Thank you. Next question is from Neha from Abacus. Please go ahead. Neha from Abacus, you may go ahead with the question. There seems to be no response on the line of Neha.
Hello?
Yes ma'am, go ahead.
Yeah, hi. Good morning and thanks for the opportunity. Two questions from my side. One is on the high other income for the standalone business for this quarter, and secondly on the overseas subsidiary business. I just wanted to understand that d o we expect the growth momentum to pick up further from here in the rest of the year, probably leading to higher leverage, only EBITDA margin per se from that particular business?
Neha, f irstly, the higher quantum of other income is largely driven by forex gains in the standalone and secondly we have guided for our overseas facilities to pick up growth momentum for the full year, and yes, we've seen that in quarter one and we do expect that momentum to continue in the second quarters as well.
Understood, thank you.
Thank you. Next question is from Tushar Manudhane from Motilal Oswal Financial Services. Please go ahead.
Thanks for the opportunity, sir. Firstly, on the other expenses, it's been a decent decrease from almost INR 620 crore in Q4 to INR 500 crore. How to think about this maybe for a full year 2026 and 2027 in terms of operational efficiencies, sort of reducing the cost or rationalizing the cost.
Firstly, let's look at the outcome. The guidance that we gave is there'll be some moderation in margin that will happen for the year. That understanding by that annual guidance and having said that, we continue to look at optimizing cost efficiencies through a program that we run within the organization, which is looking at all levers, whether it's sourcing cost, yield efficiencies, and general OpEx as well. Yes, we'll continue to see how we can keep the cost tight to the extent possible and focus on improving efficiencies thereafter.
Because let's say the on-patent commercial product could have got a good gross margin. Probably your guidance for FY 2026 EBITDA margin is to do with the reduction in the business of that on-patent molecule. I was more trying to understand on the operational cost below gross margin.
Yes, that's why you see that the operational cost is actually growing in single digits. In fact, if you exclude the impact of the forex, the growth is even much more reasonable in terms of growth visible in the previous year, Q1, if you see. Yes, we are keeping the cost under control.
Okay, and this shipment timing, is it more to do with the geopolitical tension or more about the customer facing some temporary issue of taking the product?
It's more phasing, and we do expect this to pick up in the later part of the year, more specifically in H2.
A ny other product or contract where you envisage such event happening over, say, next three to four months. Typically, the contracts are such that we have a lead time of at least three to four months to supply the product. Any other contract where you see sort of moderating?
I think nothing at the moment that we can.
Okay, thanks. Thanks a lot.
Thank you. Next question is from Suvan Mittal from MFC. Please go ahead.
Hello , thank you for the opportunity. I have two questions lined up. Firstly, being for our Sevoflurane in business CHG for anesthesia, we have done a sizable capex for rest of the world markets. Do we expect any double digit g rowth this financial year, and if yes, do we expect a sizable contribution because of the rest of world business row. Secondly, last if. Yeah, sorry, please.
I think yes, we do expect a double digit growth for the CHG business overall, and yes, some part of it will come from the rest of world business as the site continues to scale up. Yeah, it won't all be in one quarter.
For further clarity, while we had the do and tell for India and that portion of the supply from India to India can happen, a lot of the RoW do require a certain amount of stability data and a certain filing time frame. As those individual markets complete their steps, we can start serving them from this site. That will be over the year time frame, not a light switch. Yes, correct, we are able to do that out of India for India and we expect RoW to come in line country by country as an additional supply source over the year.
The second question being, in the last FY, we had maintained an EBITDA margin of u pwards of 20% for the f or three quarters at least, if you could just reconfirm, was it because of the large customer we were having?
Sorry, when you say EBITDA margin in excess of 20%, which segment are you referring to?
On an overall basis, if I'm not wrong, for two quarters we had m aintained an EBITDA margin between 18%- 23% in the last FY for Q3 and Q4.
No. If you look at even our annual full year margins, we were at 17%.
Not annual. On a quarterly basis.
On a quarterly basis we never had EBITDA margins. Only in quarter four we had EBITDA margins of close to 22%. Otherwise our margins have always been less than 20%.
Yeah.
Are you referring to the standalone then? Standalone? Yes. The margin.
Standalone, yes.
Yes, standalone margins have been in that. Yes.
For standalone basis, it could confirm. Is it because of the large customer w e were having in the CDMO business.
The standalone margins? Yes, it is because of the impact of the large customer.
Oh, okay. Thank you. Thanks a lot.
Thank you. The next question is from Chidananda Mohanty from Green Portfolio. Please go ahead.
Hello. Am I audible?
Yes, you're audible.
Yeah. My first question is what is the estimated total addressable market for Neoatricon ? The next part is that you have mentioned that the commercial agreement, which is due, t hat means are you going to cover from end to end, from manufacturing to distribution, or only distribution? I'm talking about only Neoatricon.
Yeah, we haven't. I don't believe we disclosed the TAM for this, and part of the reason is that it's a market we'll be creating because it's essentially a generic product with a differentiated product for a pediatric purpose. There is no historical market to refer to. We will create that, and as those sales happen, we will enjoy that benefit. In terms of the arrangement with our partner BrePco, they are responsible for the manufacturing of the product, and we are responsible for the sales and distribution of the product. That's the product partnership we have. In that context, they would be providing us with the product to sell, and we would be selling it.
Perfect. Perfect. The next question is, today you told that some of your products in Consumer Healthcare business has faced some price challenges and some government side. Am I following it right?
Yes. Last year the i-Pill product came under NPPA, and there was a price cut.
Came under?
The pricing authority, NPPA.
Price control.
Price control.
Who is, if I am not wrong, then are. You referring to the National List of Essential Medicine or anything else?
Yes, yes, that's it.
This was last year, not in the current year.
Yeah.
What percentage of total ICH business comes under this list?
Not very much. I think there's only the i-Pill one or two products, so not many.
Perfect, perfect. The next question is that the JV with AbbVie, that is you are targeting the ophthalmology market of India only, I mean. Correct?
Yeah.
Can you specify any quantitative number around the approximate market size? In this JV, are you developing new drugs or will only commercializing the existing drugs from both the companies?
Firstly, our JV partner and us together are responsible for manufacturing and distributing products for the India market. They are market leaders in several segments, which includes the anti-infectives, the glaucoma market, and the dry eyes as well. Currently, we are in the process of discussing what additional correct products can be added to this portfolio. You will see this in the next few years.
Thank you. Next question is from Abdulk ader Puranwala from ICICI Securities. Please go ahead.
Yeah, hi, thanks for the follow up. Just a couple of bookkeeping questions. For the quarter, the interest cost has come down significantly. If you could highlight what is creating this kind of a cost saving there, and for the full year, any color on how should we model the tax rate for this year?
Firstly, on the interest cost, there are two factors at play. One. Fairly maintained our gross debt levels, and the second is that the interest rates have seen a threat of softening. All our loans are linked to benchmark rates, whether it's SOFR overseas or the MCLR treasury bills in India. We are seeing a general trend of interest rate softening. As long as this continues, you would see a reduction in the overall interest cost. As far as the tax is concerned, we had guided for a lower effective tax rate versus what we had previously. Three factors driving that. First is the fact that we forecasted turnaround in some of our overseas facilities, which essentially means that you will have higher profits with no tax outflow given that you've got certain tax assets created.
The second part is that you will have benefits from the big beautiful bill which was signed in the U.S., which gives you an upfront deduction for your R&D investments. Of course, we continue to enjoy the benefit of R&D tax credit at our Canadian facility. Those are some of the reasons we will see a lower effective tax rate. Having said that, I am not giving a specific number because this depends upon the mix between India and overseas. You will definitely have it lower, and it depends upon the overall mix that the effective tax rate will pan out.
Got it, sir. Thank you.
Thank you. Next question is from Vibha Ravi from Citeline. Please go ahead.
Hi, this is Vibha from Citeline. I just had two broad level questions. One is that you have called out prolonged decision making by emerging biotechs in your presentation. Would you have some idea if this is in part driven by the uncertainty as to where the U.S. tariffs will land, and is there, you know, since you have an ear to the ground in your conversations, do you find that China is more and more out of the reckoning due to geopolitical concern?
I think, Vibha, the first thing I would say that funding for biotechs overall has been inconsistent over the year and it's not necessarily only related to tariffs. It would be things like the approval timelines, it would be things like fundraising and it would be things like interest rates and venture capital funding overall. I think those would be the biggest reasons rather than tariffs. I don't think I really want to comment on China.
Okay, just one more question which is there, is there any thought of your own recalibration away from the U.S. given the uncertainty and the geopolitical environment over there? Or is it too short term, a blip and it's perhaps too early to take a call there in terms of recalibration towards the domestic, towards India business?
I think overall I will say that i n the CDMO business, a lot of p eople are rethinking supply chains, and there is some thought towards reshoring or onshoring. I think we are, our network is actually well placed to capitalize on that, r ight? As a company, I don't think we will go back to the domestic India business at the moment.
Okay, thank you so much.
Thank you. Next question is from Chintan Shah from JM Financial Family Office. Please go ahead. Hi.
Thank you for the opportunity. Two questions. One is on a wanted detailed e xplanation on the EBITDA margins for this quarter. I know quarter is not very relevant, but you know one side there is a decline in this innovator volumes. On the other side, we are saying that, w e have seen better utilization, better margins for other part of the CDMO business. If we see on an overall basis, margins, if I exclude the other income, that's gone from 10.5% to 5 .5%. I just wanted to better understand this. it purely the impact because of that innovator's skills or in other segments also? Say for in CHG we have seen p ressure.
As you know, bottom one is the smallest quarter, this one has been lower. When you're looking at the overall margins, it's an aggregate mix of both the CDMO and the CHG business. You will notice that CHG, which is the highest margin business within the three verticals that we have, also has n ot grown this quarter.
While what you say in terms of impact of the on-patent commercial product not being there this quarter is true, the other fact is the CHG business has also not grown, which is also contributing to a depressed margin. As the growth restores in the CHG business in subsequent quarters, we should see this gap narrowing down.
Okay, got it. Understood. The second question is apart from this CapEx that we announced of around $90 million, any other sort of CapEx that we are looking at and broad the idea that I'm trying to get is that in order to meet our FY 2030 guidance, basically what sort of CapEx will have to do beyond this or do we have enough capacities to reach there? That's one.
Secondly, in terms of capabilities, ADCs is one where we have been actively investing. Apart from that, anything like that to call out that we're kind of investing in or focusing on or we see that could be growth drivers for us over the next four, five years.
In terms of the CapEx guidance t hat we gave for the year, we said we'd do anywhere between $100 million- $125 million. Size of the chunk of that indeed is for the announcement that we did for our North American facility, which is Lexington and Riverview. We also are investing in product development for our Complex Hospital Generics business, which is part of the basket of CapEx that we spoke about. Those will be the primary ones. Of course, besides other maintenance CapEx that we would normally do across our sites at this stage, we do expect the momentum to be in the range of about $80 million, $90 million on an average to be the kind of CapEx that we will need to kind of create or debottleneck capacities across our f acilities, w hich is part of what we have highlighted in our five year plan.
Second part on capabilities.
On the overall capability point, we've looked at what we have and what we think the market requires. At least our guidance, particularly in the area of the CDMO, is that we're looking to add capacities at our existing facilities as opposed to adding new facilities with new capabilities as our primary area of investment for the CDMO. As we look at the story that we discussed at the beginning of this call, the operating leverage and the benefits come from getting our current sites larger. In many cases, it's getting them larger with existing capabilities at current locations. We believe that that's a more effective deployment of capital strategy, especially in the short and medium term. We'll obviously look opportunistically in the medium to long term for other capabilities or geographies for existing capabilities, but at the moment it's primarily brownfield organic.
Okay, got it. Understood. That was very helpful. Thank you.
Thank you. The next question is from Harith Ahamed from Avendus Spark. Please go ahead. Hi, thanks for the opportunity.
My first question is on the Consumer Healthcare business where we have an arrangement to distribute brands from there. Is this a material part of the segment, and what is the outlook for it? This particular piece within Consumer Healthcare? When you give the $200 million. Guidance for FY 2030, is this particular revenue stream a part of it or will d o $200 million excluding this?
I think i t's 35% of the business currently. I think.
40%.
40% part of the business currently, but overall it's doing well. It grew in double digits this year, and we fully expect this arrangement to continue.
Okay, thanks for that. My second question is around the profitability a t some of our overseas facilities. When I look at the subsidiary f inancials for FY 2025, some of these units have seen a decline in margins or absolute EBITDA w hile we were expecting some improvement last year, can you give some color on what led to the decline in some of these in profitability at some of t hese facilities like Riverview, Sellersville, Lexington, and what is the outlook for this year?
Firstly, Harith, as you rightly mentioned, it was a mixed performance. You did see improvement in the performance of some of the sites like Lexington, as you alluded to. Yes, some sites did see a slightly lower margin or a decline in margin. This is a mix of both some clinical attrition or lower orders as a result of the ongoing biotech funding inconsistencies that we have been seeing. Having said that, I think it's important that we've spoken about seeing an improvement of this in FY 2026 and several of the sites. We are working towards ensuring that their execution and deliveries are improving, and thereafter the order book is also moving in the right direction.
Yes, we did have a mixed year last year and we are working towards improving performance of some of the overseas sites, the traction of which we have seen in quarter one and hopefully we should continue that in the quarters ahead.
Okay, thanks. Last one. Given the slightly muted overall margins that we are expecting for the year and the capex visibility that we have, is there any guidance that you can give on the net debt levels what we are expecting towards the end of FY 2026?
Currently, we are at 2.6 net debt to EBITDA levels, and given the fact that we've announced capex of close to $100 million- $125 million, that is the plan for the year. We will see some increase in these levels, but eventually we stand by the long-term guidance of bringing it down to net debt to EBITDA of one by FY 2030. You may see some temporary spike that may happen.
All right, that's all from my side. Thank you for taking my question.
Thank you very much. That was the last question in queue. I would now like to hand the. Conference over to Mr. Gagan Borana for closing comments.
Thank you very much. We hope we were able to answer. Most of your questions. In case you have any follow-up. Questions or any clarification, please feel free to reach out to me, and I'll be happy to respond. Thank you and have a good day.
Thank you very much on behalf of Piramal Pharma Limited, t hat concludes the conference. Thank you for joining us, ladies and gentlemen. You may now disconnect your lines.