Tag: Pharmaceutical GMP violations

Understanding GMP Regulations in Asia: A Guide to PMDA, NMPA, and KFDA

January 20, 2025 digi

Understanding GMP Regulations in Asia: A Guide to PMDA, NMPA, and KFDA A Detailed Guide to GMP Regulations in Asia: PMDA, NMPA, and KFDA Introduction to GMP in Asia In the pharmaceutical industry, Good Manufacturing Practices (GMP) are essential for ensuring product quality, safety, and efficacy. Asia, home to some of the world’s largest pharmaceutical…

GMP in Asia (PMDA, NMPA, KFDA)

GMP in Emerging Markets (GCC, Latin America, Africa)

January 20, 2025 digi

GMP in Emerging Markets (GCC, Latin America, Africa) Exploring GMP Compliance in Emerging Markets: GCC, Latin America, and Africa Introduction to GMP in Emerging Markets Good Manufacturing Practices (GMP) are fundamental to the pharmaceutical industry, ensuring the safety, efficacy, and quality of medicinal products. While developed markets have well-established GMP frameworks, emerging markets such as…

GMP in Emerging Markets (GCC, Latin America, Africa)

GMP in Asia (PMDA, NMPA, KFDA)

January 20, 2025 digi

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…

GMP in Asia (PMDA, NMPA, KFDA)

The Role of Schedule M Revised in Enhancing Drug Quality in India

January 19, 2025 digi

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…

GMP in India

Overview of Schedule M Revised: Impact on GMP Compliance in India

January 19, 2025 digi

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…

GMP in India