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    ERIS Lifescience

    ERIS
    Healthcare·20 May 2026
    Management Summary

    Eris Lifesciences reported strong Q4 and FY26 results, driven by robust performance in Domestic Formulations, particularly the Insulin and Derma segments, and a successful Semaglutide launch. Despite regulatory delays impacting new product launches and international business, the company achieved significant PAT growth and maintained healthy margins. Management outlined plans for continued growth, margin improvement through insourcing, and resolution of regulatory observations.

    Highlights

    5
    • Full year DBF revenue reached INR 2,778 crores, growing 11% YoY.

    • Full year DBF EBITDA was INR 1,026 crores, a 12% YoY growth, with margin expanding to 37%.

    • Consolidated PAT from continuing operations grew 34% YoY to INR 498 crores for FY26.

    • Eris ranked #1 in Injectable Semaglutide by sale volume in April '26, demonstrating strong platform strength.

    • Insulin segment performance was strong, with RHI cartridge market share increasing from 13% to 24%.

    Concerns

    5
    • Revenue loss of INR 55-60 crores in FY26 due to abandoned or delayed new launches (gSaxenda, Aspart, Esaxerenone) caused by regulatory delays.

    • Insulin segment incurred a sale loss of around INR 50 crores in FY26 due to delayed in-sourcing and commercial manufacturing from Bhopal.

    • International business Q4 revenue was INR 86 crores against a plan of INR 115 crores, with INR 30 crores of finished goods unshipped due to supply chain disruptions.

    • EU GMP inspection resulted in noncompliance observations, delaying commercialization of EU CDMO products and postponing INR 120-140 crores of FY27 revenue.

    • OAD segment showed minimal growth (2-4%), acting as a drag on ex-Insulin business performance.

    Key financials

    Metrics

    10

    Periods

    2

    Headline

    3
    • DBF Revenue
      ₹671 Cr
      YoY+12%
    • DBF EBITDA
      ₹246 Cr
      YoY+10%
    • DBF EBITDA Margin
      37%

    FY26

    7
    • DBF Revenue
      ₹2,778 Cr
      YoY+11%
    • DBF EBITDA
      ₹1,026 Cr
      YoY+12%
    • DBF EBITDA Margin
      37%
    • Consol Revenue
      ₹3,129 Cr
      YoY+8%
    • Consol EBITDA
      ₹1,120 Cr
      YoY+10%

    Segment breakdown

    International Business
    ₹86 Cr Q4 Revenue₹28 Cr Q4 EBITDA32.4% Q4 EBITDA Margin₹348 Cr FY26 Revenue₹110 Cr FY26 EBITDA32% FY26 EBITDA Margin
    List

    Capital allocation

    3
    high confidence
    CategoryHeadline
    Capex

    ₹300 crores

    Debt

    Net ₹2,255 crores · 2.0x EBITDA

    Liquidity

    Liquidity disclosed

    OCF to EBITDA ratio came in at close to 50% for the financial year versus 105% for the last financial year.

    Guidance & targets

    12
    CategoryTargetPriority
    Revenue
    DBF Revenue Growth
    1.3x of covered market growth
    High
    Revenue
    International Business Revenue Growth
    18-20%
    High
    Revenue
    EU CDMO Revenue Postponement
    INR 120-140 crores
    High
    Profitability
    DBF EBITDA Margin
    37%
    High
    Profitability
    DBF H2 Margin
    higher than H1
    High
    Profitability
    International Business EBITDA Margin
    similar levels as FY26
    High
    Profitability
    Consolidated ROCE
    23-25%
    High
    Product Launch
    EU CDMO Products Commercialization
    post re-inspection and re-approval
    Medium
    Product Launch
    Insulin Aspart Launch
    launching in FY27
    High
    Capacity
    SEMA Pen Manufacturing Insourcing
    5 million units per annum
    High
    Capacity
    Bhopal Cartridge Line Online
    H2 2027
    High
    Tax
    Effective Book Tax Rate
    21%
    High

    EU CDMO Commercialization Progress

    Next quarter / FY27
    CurrentINR 120-140 crores of FY27 revenue postponed due to EU GMP re-inspection pending.
    TargetProgress on re-inspection and re-approval, leading to commercialization of EU CDMO products.

    Why it matters

    Unlocks significant postponed revenue and validates the international business strategy post-remediation.

    The EU CDMO products will get commercialized post the re-inspection and re-approval of the facilities. (Page 4)

    How to verify

    guidance_and_targets[category='Product Launch'][metric='EU CDMO Products Commercialization']

    Risks & concerns

    6
    RiskSeverity

    Regulatory delays impacting new product launches

    Revenue loss of INR 55-60 crores in FY26 due to abandoned or delayed launches of gSaxenda, Aspart, and Esaxerenone.Management acknowledged

    medium

    Delayed in-sourcing and manufacturing for Insulin products

    Sale loss of around INR 50 crores in FY26 due to delays in in-sourcing and commercial manufacturing from Bhopal.Management acknowledged

    medium

    International business supply chain disruptions

    INR 30 crores of finished goods could not be shipped in Q4, leading to a miss in international business revenue targets.Management acknowledged

    medium

    EU GMP inspection non-compliance and delayed CDMO commercialization

    Noncompliance observations from EU GMP inspection are delaying commercialization of CDMO products, postponing INR 120-140 crores of FY27 revenue.Management acknowledged

    medium

    Underperformance of OAD segment

    OAD segment growth was minimal (2-4%), acting as a drag on the overall ex-Insulin business growth.Management acknowledged

    medium

    H1 FY27 gross margin pressure

    H1 FY27 is expected to have a 'drag' on gross margins, partly due to initial Semaglutide launch expenses.Management acknowledged

    medium

    Q&A highlights

    8

    “Now OAD, we had a Glimisave MV banned last year, which was INR 30 crore in revenue for us, which internally is, like 4.5%. So, what will you see is that that ban happened in the month of April last year. It looks. So, by May, what will you see that the base correction would happen. So that is only one thing. But, you know, the way April, May is shaping up, we can tell you that, you know, your logic might not be correct. We are seeing a little bit of a, you know, rebound in OAD, and then we are launching a couple of more products, the Esaxerenone, which I spoke about later. So, I think ex-Insulin double digit growth is something which could be easily achieved.”

    Clarifies that the perceived lower ex-Insulin growth was due to specific OAD segment issues and new launches are expected to drive double-digit growth.

    asked by Kunal Randeria

    3 min read6 chapters

    Detailed Narrative

    01

    Q4 and Full Year FY26 Financial Performance Overview

    Eris Lifesciences reported a strong Q4 and full year FY26. Domestic Formulations Business (DBF) revenue grew 12% in Q4 to INR 671 crores and 11% for the full year to INR 2,778 crores. DBF EBITDA for Q4 was INR 246 crores (10% growth) with a 37% margin, while full year DBF EBITDA reached INR 1,026 crores (12% growth) with a 37% margin, up from 36.5% in FY25. Consolidated revenue for FY26 was INR 3,129 crores, an 8% growth, and consolidated EBITDA was INR 1,120 crores, growing 10%. PAT from continuing operations for FY26 saw a significant 34% YoY growth to INR 498 crores, leading to an EPS of INR 36.

    02

    Domestic Formulations Business Drivers and Challenges

    The Domestic Formulations business saw strong performance in the Insulin and Derma segments. Insulin market share in RHI cartridges increased from 13% to 24%, and overall Insulin segment share grew from 12% to 16%, with Eris's growth of 32% outpacing the covered market by nearly five-fold. The Derma segment also outperformed, growing 14.2% against a market growth of 8.6%. However, the company faced challenges, including a revenue loss of INR 55-60 crores from delayed new launches (gSaxenda, Aspart, Esaxerenone) and a INR 50 crore sale loss in the Insulin segment due to delayed in-sourcing. The OAD segment's minimal growth (2-4%) also acted as a drag.

    03

    Semaglutide (Sundae) Launch and Market Strategy

    Eris's Semaglutide brand, Sundae, had a robust start following its launch. In April '26, Eris ranked #1 in Injectable Semaglutide by sale volume and #2 by sale value. The company achieved a 22% prescription market share in May for Injectable SEMA. Sundae Vials were launched in March, followed by Sundae Pen 2mg in mid-April and 4mg in early May. The product is priced competitively at INR 1,290 per unit for Vials and INR 3,200 per unit for Pens, which is 30% lower than most competitors. Management expects tailwinds from Q2 FY27 as insourced manufacturing of Sundae Pens with a 5 million units per annum capacity comes online, promising eased supply and margin improvement.

    04

    International Business Performance and EU GMP Inspection

    The International business faced headwinds in Q4, with revenue reaching INR 86 crores against a plan of INR 115 crores, primarily due to INR 30 crores of finished goods being unshipped due to supply chain disruptions. For the full year, international revenue grew 7% to INR 348 crores, with an EBITDA margin of 32%. The company received noncompliance observations from a recent EU GMP inspection, which were largely procedural. While remediation is a priority and underway, this has postponed INR 120-140 crores of EU CDMO revenue from FY27. Management guides for 18-20% revenue growth in FY27 for the existing international business, with similar EBITDA margins.

    05

    Capital Allocation and Efficiency Improvement

    Eris's capital expenditure for FY26 was close to INR 300 crores, primarily directed towards Biologics and Sterile Injectables, including INR 150-180 crores for DS capacity and INR 250 crores for the Bhopal fill and finish site. The closing net debt for FY26 was INR 2,255 crores, representing 2x EBITDA, and finance costs were down 17% YoY. The OCF to EBITDA ratio improved significantly to 50% for FY26 from 105% in the prior year. Management expects the return on capital employed (ROCE) to improve from 15% to 23-25% over the next three years (FY26-FY28) as these strategic investments begin to yield returns.

    06

    Working Capital Management and Outlook

    The company observed an increase in inventory and receivables during the year. Inventory buildup was attributed to strategic stock-up of key APIs due to price volatility and unshipped finished goods in the international business due to Q4 disruptions. Receivables also increased, with management targeting to bring debtor days down to around 60 days within the next two quarters. Despite these temporary increases, management expressed confidence in normalizing working capital metrics and stated there is no risk of bad debt.

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