Akums Drugs & Pharmaceuticals Ltd., an India-based CDMO, has secured European Union Good Manufacturing Practice (EU GMP) certification for two of its manufacturing facilities located in India.

The EU GMP certification includes renewal for its oral solid dosage facility (tablets, capsules and sachets) and fresh certification for its oral liquid facility (solutions, syrups and suspensions). These approvals enhance Akums’ ability to serve regulated European markets while adhering to globally benchmarked quality and compliance standards.

With a long-term vision of being a recognized household name across EU and UK markets, Akums has marked its entry in UK Market with its first UK MHRA approval for Rivaroxaban. This approval marks Akums’ direct entry into the UK anticoagulant market.

Commenting on the milestone, Mr. Sandeep Jain, Managing Director, said: “We built scale, compliance and credibility in India. Our vision now extends with the same commitment to Europe and the UK. What we have achieved domestically, we are determined to replicate globally—with quality, reliability and long-term partnerships.”

Currently serving 1,500+ clients worldwide, Akums operates 14 world-class plants comprising 12 formulation manufacturing facilities and 2 API plants, with a collective production capacity exceeding 50+ billion units annually.