Mastering Quality: A Practical Guide to QMS in the Pharmaceutical Industry

Description

This comprehensive eBook explores the principles, components, and regulatory expectations of Quality Management Systems (QMS) in the pharmaceutical industry. From GMP compliance to risk management, CAPA, documentation control, validation, and audit readiness, the guide provides actionable insights for professionals striving to maintain high standards of quality and regulatory compliance. Whether you’re a quality officer, validation engineer, regulatory affairs professional, or plant manager, this resource will help you implement and improve QMS effectively in your pharmaceutical operations.