Alkem Laboratories receives EU GMP Certificate for Baddi facility
Alkem Laboratories received an EU GMP Certificate for its Baddi manufacturing facility from Germany's Department of Pharmacy. The certificate is valid for three years post-inspection, which occurred from Nov 4-10, 2025.
The EU GMP certification is significant for a pharmaceutical company as it validates manufacturing standards and can facilitate access to European markets, impacting future sales and regulatory standing.
Receipt of a GMP certificate from a European regulatory authority is a positive development, indicating compliance and potentially opening up new market opportunities.
Alkem Laboratories Limited has received a 'Certificate of GMP Compliance of a Manufacturer' from the Department of Pharmacy (Human Medicines) – Germany. This certificate follows an inspection conducted at the company's manufacturing facility located in Baddi, India, from November 4, 2025, to November 10, 2025. The certificate is valid for three years from the date of inspection. This intimation is in furtherance to the company's earlier disclosure dated November 10, 2025, regarding the EU GMP inspection by the German Health Authority.
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