BSECompany Update2d ago · 23 Sept 2026, 08:46 am
Glenmark Pharmaceuticals receives Establishment Inspection Report (EIS) from U.S. FDA for its Goa facility with VAI classification
Glenmark Pharmaceuticals Ltd · 532296
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Glenmark Pharmaceuticals Ltd has received the Establishment Inspection Report (EIR) from the U.S. FDA for its Goa facility with a Voluntary Action Indicated (VAI) status.
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Glenmark Pharmaceuticals Ltd - 532296 - Announcement under Regulation 30 (LODR)-Press Release / Media Release
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September 23, 2026
To, To,
National Stock Exchange of India Limited, BSE Limited,
“Exchange Plaza”, Corporate Relationship Department,
5th Floor, Plot No. C/1, G Block, 2nd Floor, New Trading Ring,
Bandra- Kurla Complex, Bandra (East), P.J. Towers, Dalal Street,
Mumbai – 400 051 Mumbai – 400 001
Scrip Name: GLENMARK Scrip Code: 532296
ISIN: INE935A01035 ISIN: INE935A01035
Our Reference No. 57/26-27 Our Reference No. 57/26-27
Dear Sir/ Madam,
Sub: Glenmark Pharmaceuticals receives Establishment Inspection Report (EIR) from U.S. FDA for its
Goa facility with VAI classification
Glenmark Pharmaceuticals Ltd (Glenmark), a research-led, global pharmaceutical company today
announced that it has received the Establishment Inspection Report (EIR) from the U.S. Food and Drug
Administration (U.S. FDA) for its formulations manufacturing facility in Goa, India with a Voluntary Action
Indicated (VAI) status.
Kindly find attached media release which is self- explanatory.
Request you to take the same on record.
Thanking you.
For Glenmark Pharmaceuticals Limited
Rashmi Khandelwal
Company Secretary & Compliance Officer
ACS – 28839
Encl: As above
Glenmark Pharmaceuticals Limited
Glenmark House, B D Sawant Marg, Andheri (E), Mumbai 400 099
T: 91 22 4018 9999 F: 91 22 4018 9988 CIN No: L24299MH1977PLC019982 W: www.glenmarkpharma.com
Registered office: B/2, Mahalaxmi Chambers, 22 Bhulabhai Desai Road, Mumbai 400 026 E: complianceofficer@glenmarkpharma.com
Glenmark Pharmaceuticals receives Establishment Inspection
Report (EIR) from U.S. FDA for its Goa facility with VAI
classification
Mumbai, September 23, 2026: Glenmark Pharmaceuticals Ltd (Glenmark), a research-led,
global pharmaceutical company today announced that it has received the Establishment
Inspection Report (EIR) from the U.S. Food and Drug Administration (U.S. FDA) for its
formulations manufacturing facility in Goa, India with a Voluntary Action Indicated (VAI) status.
The inspection was conducted at the Company’s manufacturing facility from June 22, 2026 to
June 30, 2026.
About Glenmark Pharmaceuticals Limited
Glenmark Pharmaceuticals Ltd. (BSE: 532296 | NSE: GLENMARK) is a global, research‐led pharmaceutical
company with a unique focus on innovation and accessibility. We pioneer transformative breakthrough therapies
that aim to redefine treatment while expanding access to high-quality and affordable medicines for patients around
the world. With 11 world-class manufacturing facilities across four continents, supported by six cutting-edge R&D
centres, and a commercial footprint in 80+ countries, we deliver a diversified portfolio across branded, innovative,
generics, and consumer health products, with a focus on respiratory, dermatology, and oncology. Scrip 100
positions Glenmark among the Top 100 biopharmaceutical companies globally by pharmaceutical sales for 2024.
For more information, visit www.glenmarkpharma.com
For more information, please contact:
Akhila Natarajan | mediarelations@glenmarkpharma.com | +91 22 4018 9999
Adfactors PR | glenmark.ihcp@adfactorspr.com |+91 95356 35461