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《中华人民共和国药品管理法实施条例》颁布施行,是我国药品监督管理法制建设中的一件大事。《实施条例》的正式施行,使得《药品管理法》更具可操作性,同时也对药品监督执法主体提出了更高的要求。在此,本刊摘登了北京市药监局稽查处提供的几则案例,文章对销售假药案、无证经营药品案、药品抽验不合格案等案例进行了扼要分析,供大家互相学习、参考、借鉴,以不断提高依法监管的水平和效率。
The promulgation and implementation of the “Regulations for the Implementation of the Drug Administration Law of the People’s Republic of China” are a major event in the legal construction of pharmaceutical supervision and administration in our country. The formal implementation of the “Implementing Regulations” made the “Drug Administration Law” more feasible and also put forward higher requirements on the subject of drug regulatory law enforcement. Here, we published several cases provided by the Audit Office of the Beijing Food and Drug Administration Bureau. The article has a brief analysis of the cases of sales of counterfeit drugs, drug-free drugs and drug sampling substandard cases so that students can learn from each other, Reference, reference, in order to continuously improve the level and efficiency of supervision according to law.