Alkem Labs receives EU GMP Certificate for Daman facility from Malta Medicines Authority
Alkem Laboratories has received an EU GMP Certificate from the Malta Medicines Authority for its Daman manufacturing facility. The certificate is valid for three years from December 9th, 2025.
The EU GMP certification is significant for expanding market reach and can positively impact future revenue streams, although the immediate financial impact is not quantified.
Receipt of an EU GMP certificate indicates compliance with European Union standards, which is positive for the company's export capabilities and market access.
Alkem Laboratories Limited has received a 'Certificate of GMP Compliance of a Manufacturer' from the Malta Medicines Authority for its manufacturing facility located in Daman, India. This certificate is valid for three years from the inspection date of December 9th, 2025.
This development follows an earlier intimation on December 10th, 2025, regarding a GMP inspection conducted by the Malta Medicines Authority at the Daman facility. The company will make a copy of this disclosure available on its website as per SEBI LODR Regulations.
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