Explanation of Chinese Pharmaceutical Laws and Regulations

Author: Yang Shimin
Publisher:
Publish Date: 2004-02-01
Features: "Interpretation of Chinese Pharmaceutical Laws and Regulations" explains 21 current pharmaceutical laws and regulations, including the "Drug Administration Law of the People's Republic of China," the "Implementation Rules for the Drug Administration Law of the People's Republic of China," the "Drug Registration Management Measures," the "Good Manufacturing Practice for Drugs," the "Good Supply Practice for Drugs," the "Provisional Regulations on Pharmaceutical Affairs Management in Medical Institutions," and the "Provisional Regulations on the Qualification System for Licensed Pharmacists." Each regulation is explained independently, covering the purpose and significance of legislation, the background of the regulation's issuance, main content, and explanations of common terms. It also compares the old and new content of amended regulations. Some regulations have been supplemented with explanatory documents or additional rules after implementation, which are also introduced in this book to reflect the latest developments and progress in China's pharmaceutical laws and regulations. The book is characterized by its novel content, emphasis on key points, and strong practicality. It is suitable for pharmaceutical regulatory personnel, pharmaceutical technicians in research, production, distribution, use, and testing departments, as well as students of higher medical institutions for reference and study.