Medicinal Products Regulatory Brief Glossary

Author: Sun Dongfeng et al. (Editor-in-Chief)
Publisher:
Publishing Date: 2003-12-01
Features: To ensure the safe and effective use of medications by the public and meet the needs of pharmaceutical supervision and market economic development, this book takes the "Drug Administration Law" as the main thread, combining practical pharmaceutical supervision with the practice of modern medicine, traditional Chinese medicine, pharmaceutical administration, drug quality supervision, and relevant laws and regulations. It systematically categorizes and explains common terms, striving to be scientific, novel, comprehensive, and systematically annotated. It is available for use and reference by pharmaceutical supervision personnel at all levels, grassroots pharmaceutical administration and inspection workers, pharmaceutical producers and operators, students of medical and pharmaceutical institutions, legal professionals, rural doctors, and others.