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《药品管理法》的颁布实施,标志着我国药品监督管理工作走上了法制化轨道.这是党和国家为加强药品管理,保障人民健康做出的重要决策.多年来,药品质量的监督,主要是药品检验所通过检验成品对药品质量进行控制.但现代质量管理理论认为,它包括药品从研究开发、投入生产、质量检验、流通渠道、到最后用于临床使用等所有环节,都涉及到如何控制药品质量问题.因此,当前药品监督管理工作主要任务是以《药品管理法》为法律依据,对药品生产、供应、使用部门及市场游散药贩进
The promulgation and implementation of the Drug Administration Law marks the beginning of the legalization of pharmaceutical supervision and administration in our country, which is an important decision made by the party and the state to strengthen drug administration and safeguard people’s health. Over the years, the supervision of drug quality, Mainly through the inspection of pharmaceutical products by the finished product on the quality of pharmaceutical control, but the modern quality management theory that it includes drugs from research and development, into production, quality inspection, distribution channels, and finally for clinical use and all other aspects are involved How to control the quality of the drugs.Therefore, the main task of the current drug supervision and management is based on the “Drug Administration Law” as the legal basis for the drug production, supply, use department and the market to travel bulk drug trafficking