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GMP in Asia (PMDA, NMPA, KFDA) A Comprehensive Overview of GMP Regulations in Asia: PMDA, NMPA, and KFDA Introduction to GMP in Asia The pharmaceutical industry in Asia is governed by stringent Good Manufacturing Practices (GMP) to ensure the safety, efficacy, and quality of medicinal products. Regulatory authorities such as Japan’s Pharmaceuticals and Medical Devices…
The Role of Schedule M Revised in Enhancing Drug Quality in India How Schedule M Revised is Improving Pharmaceutical Product Quality in India Introduction to Schedule M Revised and Drug Quality The quality of pharmaceutical products is paramount for ensuring patient safety and effective treatment outcomes. In India, the revision of Schedule M under the…
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Overview of Schedule M Revised: Impact on GMP Compliance in India Understanding the Revised Schedule M: Enhancing GMP Compliance in India Introduction to Schedule M Revised Schedule M of the Drugs and Cosmetics Rules, 1945, outlines the requirements for Good Manufacturing Practices (GMP) for pharmaceuticals in India. The recent revisions to Schedule M have introduced…
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