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依据《中华人民共和国药品管理法》第九章关于药品监督的规定,为加强对药品生产企业、经营企业和使用单位的药品质量的监督、检查工作,特制定《药品监督员工作条例》,现印发给你们,请遵照执行.实行药品监督员制度,是我国药品监督管理工作法制化的重要措施,药品监督员队伍是建立健全药品的国家监督保证体系的组成部分.各级卫生行政部门要在人民政府的领导下,加强对药品监督员的管理,做好药品监督
According to Chapter Nine of the Drug Administration Law of the People’s Republic of China on Drug Supervision, in order to strengthen the supervision and inspection on the quality of medicines of pharmaceutical manufacturers, enterprises and users, the “Regulations on the Work of Drug Supervisors” is hereby formulated It is an important measure for the legalization of pharmaceutical supervision and administration in our country and the team of drug supervisors is an integral part of establishing and perfecting the national supervision and assurance system of medicines. Under the leadership of the People’s Government, the management of drug supervisors should be strengthened and medicines should be supervised