Pharmaceutical GMP Documentation Tutorial

Author: Li Jun (Compiler)
Publisher:
Publishing Date: 2002-01-01
Features: This book is designed to meet the needs of red enterprises for the implementation and certification of GMP, as well as the establishment of a robust document system. Based on China's GMP (revised in 1998) as the benchmark and guided by the ISO 9000 family of international standards and the ISO 14000 series standards, it provides a practical and theoretical training textbook for employees in pharmaceutical companies, especially those responsible for document preparation. The book is divided into three parts: Introduction, Theory, and Practice, with detailed discussions on the theme of GMP document preparation across 15 chapters. The content is rich and the information is comprehensive. It can be used as a reference for hospital preparation rooms, as well as for medical device, food, and cosmetic manufacturers.