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药品是人们与疾病作斗争的武器,管之有方,用之得当,可为人民防病治病,如果失之管理,粗制滥造,质量低劣,则危害人民身体健康,甚至危及生命。因此,1985年7月1日我国颁布实施了《药品管理法》,标志着我国药品监督管理工作进入了法制化轨道。为了进一步深入贯彻执行《药品管理法》,强化药品监督检查工作,笔者就如何开展基层药品质量监督工作进行探讨。广泛宣传贯彻执行《药品管理法》,强化药品监督
Drugs are the weapons to fight diseases. They are well-managed and can be used by people for prevention and treatment of diseases. If they are not managed properly, their quality is poor, they will endanger people’s health and even endanger lives. Therefore, on July 1, 1985, China promulgated and implemented the “Drug Administration Law”, marking that our country’s drug regulatory work has entered a legal orbit. In order to further implement the “Drug Administration Law” and strengthen drug supervision and inspection work, the author discusses how to carry out quality control of grassroots drug products. Extensive publicity and implementation of “Drug Administration Law” and strengthen drug supervision