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Glenmark Pharmaceuticals gets EIR with VAI status for Goa facility
Sep-23-2026

Glenmark Pharmaceuticals has received the Establishment Inspection Report (EIR) from the U.S. Food and Drug Administration (USFDA) 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.

Glenmark Pharmaceuticals is a global research-led pharmaceutical company with presence across Generics, Specialty and OTC business with operations in over 50 countries.


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