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Akums Secures Dual EU GMP Certification for Haridwar Facilities.

On Monday, February 23, 2026, Akums Drugs & Pharmaceuticals Ltd., India’s largest Contract Development and Manufacturing Organization (CDMO), announced that it has secured European Union Good Manufacturing Practice (EU GMP) certification for two of its major facilities in Haridwar, Uttarakhand.

This dual certification is a significant regulatory leap, combining a successful renewal for its oral solids plant with a first-time “fresh” certification for its oral liquids facility.


Facility Breakthroughs: Haridwar Hub

The audits, conducted by the Bulgarian Drug Agency (BDA), validate Akums’ adherence to the world’s most stringent quality benchmarks.


Strategic UK Entry: Rivaroxaban Approval

Parallel to the EU GMP milestone, Akums has secured its first UK MHRA (Medicines and Healthcare products Regulatory Agency) approval for Rivaroxaban, an oral anticoagulant used to treat blood clots.


Scale and Capacity (2026)

With these new approvals, Akums is leveraging its massive domestic base to fuel global exports.

MetricStatus
Total Facilities14 Plants (12 Formulation, 2 API units).
Annual Capacity50+ Billion units (Formulations) and 737 MT (APIs).
Workforce16,000+ personnel.
Global ReachServing 1,500+ clients across 65+ countries.
Revenue (Q3 FY26)₹1,160 Crore (up 14.8% YoY).

Leadership Perspectives

“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.” — Sandeep Jain, Managing Director.

“Achieving certification across two facilities simultaneously underscores the maturity of our compliance and operational capabilities. This enables our partners to rely on us for consistent quality across multiple dosage forms.” — Sanjeev Jain, Co-Managing Director.


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