Pharmacology Chapter 20
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药品生产监督管理办法Measures for the Supervision over and Administration ofPharmaceutical Production国家食品药品监督管理总局State Food and Drug Administration药品生产监督管理办法Measures for the Supervision over and Administration of Pharmaceutical Production (2004年8月5日国家食品药品监督管理局令第14号公布根据2017年11月7日国家食品药品监督管理总局局务会议《关于修改部分规章的决定》修正)The Measures for the Supervision over and Administration of Pharmaceutical Production, which were deliberated and adopted at the executive meeting of the State Food and Drug Administration, are hereby promulgated, and shall come into force as of the date of promulgation.第一章总则Chapter I General Provisions第一条为加强药品生产的监督管理,根据《中华人民共和国药品管理法》、《中华人民共和国药品管理法实施条例》(以下简称《药品管理法》、《药品管理法实施条例》),制定本办法。
Article 1 With a view to strengthening the supervision over and administration of pharmaceutical production, the present Measures are formulated in accordance with the Pharmaceutical Administration Law of the People's Republic of China, Regulation on the Implementation of the Pharmaceutical Administration Law of the People's Republic of China (hereinafter referred to as the Pharmaceutical Administration Law, Regulation on the Implementation of the Pharmaceutical Administration Law).第二条药品生产监督管理是指食品药品监督管理部门依法对药品生产条件和生产过程进行审查、许可、监督检查等管理活动。