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Quality Management Systems in the Pharmaceutical Industry: Part-2
Dr. Nitish Bhatia
9788196848071
2024
522 pages
6*9
Hardcover
Rs. 4995

Quality Management Systems (QMS) in the Pharmaceutical sector ensure producers meet safety, Efficacy, and regulatory standards. They involve structured processes that cover all stages from Development to distribution. Key elements include compliance with Good Manufacturing Practice (GMP) and regulatory frameworks like FDA guidelines. QMS emphasizes risk management, Continuous improvement, and thorough documentation. It aims to minimize errors, prevent Deviations, and maintain product consistency. Regular audits and inspections ensure compliance and Quality assurance. A robust QMS enhances operational efficiency while safeguarding patient health. Ultimately, it supports regulatory reporting and ensures adherence to global quality standards.