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为加强医疗机构药品监督管理,健全药品质量保证体系,强化医疗机构药品质量意识,保障人民群众用药安全,依据《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》,国家食品药品监督管理局制定了《医疗机构药品监督管理办法(试行)》,于2011年10月11日发布,并于发布之日起施行。《医疗机构药品监督管理办法(试行)》对医疗机构药品的购进、储存、调配、使用等行为提出了规范要求,并对相关法律责任做了具体规定。为加强宣传,本刊现予以转载。
In order to strengthen supervision and administration of pharmaceuticals in medical institutions, improve the quality assurance system of pharmaceutical products, strengthen the awareness of pharmaceutical quality in medical institutions and ensure the safety of drug users, the People’s Republic of China Drug Administration Law and the Regulations for the Implementation of the Drug Administration Law of the People’s Republic of China, The Drug Administration has formulated the Measures for the Supervision and Administration of Drugs in Medical Institutions (for Trial Implementation), which was promulgated on October 11, 2011 and came into force on the day of its promulgation. The Measures for the Supervision and Administration of Drugs in Medical Institutions (for Trial Implementation) have set forth the regulatory requirements on the purchase, storage, deployment and use of medicines in medical institutions, and have specified the relevant legal responsibilities. To enhance publicity, this issue appears to be reproduced.