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Updated Manufacturing Practices for Drug Makers
January 14 , 2024
320 days
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- The Union Health Ministry notified revised rules under Schedule M of the Drugs and Cosmetics Rules, 1945.
- It was aimed at ensuring robust quality control for pharma and biopharmaceutical products.
- Schedule M prescribes the Good Manufacturing Practices (GMP) for pharmaceutical products.
- The revised Schedule M has been notified as rules to ensure GMP is adhered to, and requirements of premises, plant, and equipment for pharmaceutical products.
- GMP was first incorporated in Schedule M of the Drugs and Cosmetics Rules, 1945 in the year 1988 and the last amendment was done in June, 2005.
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