GMP一词引进我国已多年,意指“药品生产管理和质量控制规范”。 我国改革开放以来,先后出台了《药品管理法》等一系列药品及其生产管理法规条例。去年,国务院又专门下达了“关于进一步加强药品管理工作的紧急通知”。这些都有力地保证了我国医药经济的健康发展。 伴随着市场经济的逐步发展,医药生产经营管理的薄弱问题再度突出,这表现在制售假劣药品的违法 The term “GMP” has been introduced into China for many years, meaning “drug production management and quality control standards.” Since China’s reform and opening up, a series of drugs such as the “Drug Administration Law” and its production management regulations have been introduced. Last year, the State Council issued another “Emergency Circular on Further Strengthening Drug Administration.” These efforts have ensured the healthy development of China’s pharmaceutical economy. With the gradual development of the market economy, the weak issue of pharmaceutical production and operation and management has become prominent again. This is reflected in the illegal production and sale of counterfeit and inferior drugs.