BSECompany Update6 Oct 2026 · 6 Oct 2026, 05:30 pm
Transcript of the Webinar held on September 29,2026
Granules India Ltd-$ · 532482
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Granules India Ltd held a webinar to discuss its growth strategy and transformation plans, highlighting four growth engines: control substances, complex generics and early market opportunities, oncologies, and peptide CDMO. The company aims to translate investments into a larger business with faster earnings growth over the next three to four years while maintaining financial discipline.
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Granules India Ltd-$ - 532482 - Transcript Of The Webinar
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Date: October 06, 2026
National Stock Exchange of India Limited
BSE Limited
Symbol: NSE: GRANULES: BSE: 532482
Dear Sir,
Subject: Transcript of the Webinar.
Ref: Our letter dated September 26, 2026 for intimation of the schedule of webinar.
Pursuant to regulation 46 of the SEBI (Listing Obligations and Disclosure Requirements)
Regulations, 2015, the transcript of the webinar held on September 29, 2026 is enclosed with this
letter.
Kindly take the above information on record.
For GRANULES INDIA LIMITED
CHAITANYA TUMMALA
(COMPANY SECRETARY &
COMPLIANCE OFFICER)
REGISTERED OFFICE
Granules India Limited
CIN: L24110TG1991PLC012471
15th
Floor, Granules Tower, Botanical Garden Road, Kondapur, Hyderabad – 500084, Telangana, India
Contact Us: Tel: +91-40-69043500 |Fax: +91-40-23115145| mail@granulesindia.com
www.granulesindia.com
Granules India Limited
The Now & The Next
September 2026
- Ms. Tanvi:
- We are live now, Naman, I hand it over to you.
- Mr. Naman Bagrecha – IIFL Capital Services Limited:
- Thank you Tanvi. Good afternoon everyone. On behalf of IIFL Capital Services Limited,
we welcome you all to Granules India 2.0 Comprehensive Transformation Underway
webinar with Granules promoters and senior management team to understand the key
growth engines. We will begin the call with the opening commentary from Dr. Krishna
Prasad Chigurupati, Chairman and Managing Director, followed by Ms. Priyanka
Chigurupati, ED, Mr. Vijay, President Granules Pharmaceuticals, Inc., Mr. Sanjay Kumar,
CEO Senn Tides India Private Limited, and Mr. Mukesh Surana, CFO Granules, which will
be followed by a Q&A session. Over to you, doctor.
- Dr. Krishna Prasad Chigurupati - Chairman & Managing Director, Granules India
Limited:
- Thank you, Naman, and a very good afternoon everyone, and thank you very much for
joining us today. Over the last few years, many conversations around Granules have
understandably focused on regulatory journey, our earnings quality, earnings recovery,
and the challenges we face as an organization. Today, I would like to shift that
conversation. I would like to spend a few minutes talking about what comes next for
Granules.
- After nearly three years of relatively flat performance, we returned to growth in FY26.
For me, this was a very important milestone, but I view it not as a destination, but the
beginning of a new journey and a growth cycle for the company. Over the last several
years, we have invested significantly in manufacturing infrastructure, in R&D, in product
development, and building new capabilities. Today, we are moving from building these
capabilities to scaling them and converting them into commercial growth. The slide you
see in front of you captures how we think about this journey.
- At the foundation is our established business built on manufacturing excellence, vertical
integration, scale, and cost competitiveness. This business remains central to Granules.
It generates cash, supports our balance sheet, and provides a platform from which we
can invest in future growth. Building on that foundation, we have identified four growth
engines, control substances, complex generics and early market opportunities,
oncologies, and peptide CDMO. These are not four independent bets. They are built on
capabilities we already possess while giving us multiple venues for growth across
different products, markets, and timelines.
- Beyond these growth engines, we continue to evaluate additional opportunities and
expand our geographic reach. Because even as today's businesses scale up, we must
continue building the next generation of growth. Our objective over the next three to
four years is straightforward. To translate these investments into a substantially larger
business with earnings growing faster as our portfolio becomes more differentiated and
operating leverage develops. And equally importantly, we intend to do so while
maintaining the financial discipline that has always been fundamental to Granules.
- With that context, let me hand over to Priyanka who will take you through our product
strategy, R&D priorities, and opportunities that exist. Over to you, Priyanka.
- Ms. Priyanka Chigurupati – Executive Director, Granules India Limited:
- Thank you, CMD. You've outlined the four engines of our next growth cycle. I'd like to
focus a little bit on portfolio, R&D strategy, and market strategy that underpins this
transformation. Our next phase is not simply about efficient manufacturing at scale and
selling more products. It's about generating greater value from each successful
development program. Our vertically integrated manufacturing platform remains the
foundation. What is changing is, how we deploy that foundation and our R&D
capabilities to capture new growth opportunities.
- Our evolving growth strategy. The next phase of growth is fundamentally different from
the last. While scale, manufacturing, efficiency, and cost competitiveness have been
central to our success, while we continue to nurture them, the future growth is
increasingly going to be driven by higher value products, with products being extended
to other markets, an improved portfolio mix, and greater operating leverage. Over the
past several years, we've invested significantly in R&D, manufacturing, infrastructure,
and advanced formulation capabilities. A substantial part of this foundation is already in
place.
- Our priority now is to convert these investments into commercial opportunities and
generate greater value from our existing assets. Our vertically integrated platform
spanning APIs through to finish dosages remains a fundamental competitive advantage.
We intend to leverage this foundation not to simply increase volumes, but to develop
and manufacture more differentiated products using existing knowledge and improve
the quality of our earnings. On our portfolio transformation, perhaps the most
significant change taking place within our R&D and product development strategy is our
first-to-file playbook. Historically, growth in generics has often been associated with the
number of products developed and filed. Our approach is increasingly selective.
- Product selection is guided by technical complexity, patient needs that are unmet,
competitive intensity, intellectual property considerations, and economics of market
entry. This strategy has been demonstrated through the contribution of complex
generics that increased from 1% of overall revenue in fiscal 20 to 33% of overall revenue
in fiscal 26. And as a part of, as a percentage of overall finished dosages, the
contribution of complex is roughly 45 to 50% in fiscal 26. We are prioritizing
opportunities where our formulation expertise, vertical integration, and manufacturing
capabilities can create meaningful differentiation. We're building a broader pipeline of
differentiated opportunities across controlled substances, oncology, and other complex
generics with further filings planned over the coming years. Our first-to-file strategy is
the clearest evidence of that transformation. We've already filed two sole first-to-file
ANDAs, marking an important milestone in the evolution of our R&D capabilities.
Generic Lumryz and Generic Dyanavel have a combined market size north of 350 million
US dollars, just in the US, where we would potentially have 180-day exclusivity.
- We have filed another product, which we believe would be a sole FDF in the oncology
category. Over the next few years, we have a pipeline of four to five other first-to-files,
all of which would commercialize between fiscal 30 and 34. This reflects a clear and
visible change in Granules' R&D story. These opportunities have a different commercial
profile from conventional generics. Successful early market entry with 180-day or more
of exclusivity, particularly in products with significant technical and regulatory barriers,
can create substantial commercial value. The timing and realization of these
opportunities depend on regulatory approvals, intellectual
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