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现将我部1987年第1号药品质量抽验结果公报印发给你们.对不合格产品要及时进行处理.附件:中华人民共和国卫生部药品质量抽验结果公报卫生部1987年4月10日·附件·中华人民共和国卫生部药品质量抽验结果公报[(87)第1号(总第3号)]根据《中华人民共和国药品管理法》规定,为保障人民群众用药安全有效,维护人民身心健康,必须加强对药品生产企业、经营企业和医疗单位药品质量的监督、检查、抽验工作.
The Ministry of Health of the People’s Republic of China now publishes the results bulletin of the quality of medicines taken by the Ministry of Health of the People’s Republic of China on April 10, 1987 · Attachment · Bulletin of the People’s Republic of China Ministry of Health on Quality Inspection of Drugs [87 (87) No. 1 (No. 3)] According to the “Drug Administration Law of the People’s Republic of China”, in order to ensure people’s safety and effectiveness of drug use and safeguard people’s physical and mental health, we must strengthen Supervision, inspection and sampling of drug quality of pharmaceutical production enterprises, enterprises and medical units.