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USFDA completes GMP inspection at Glenmark Pharma’s facility at Aurangabad

21 Sep 2024 Evaluate

United States Food & Drug Administration (USFDA) completed a Good Manufacturing Practice (GMP) inspection at the Glenmark Pharmaceuticals’ formulation manufacturing facility based out of Chhatrapati Sambhaji Nagar (Aurangabad), India. The inspection was conducted from September 09 to September 20, 2024. The inspection closed with no observation.

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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