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根据1985年世界卫生组织科技交流计划,中国卫生部于1986年5月11日至6月8日派出药品标准及药典考察组赴英国和日本考察。考察目的是:了解这些国家药品标准及药典组织机构及人员情况,制订药品标准及药典的程序及原则以及新药质量标准审批情况等,从中吸取有用的经验,以促进我国药品标准及药典的编制工作,提高药品标准水平,并通过考察,建立与国外同行的联系和有大的技术情报交流。考察组由卫生部江焕波副局长领队,组员有药典委员会秘书杨岱、天津药检所所长黄乔书、辽宁省卫生厅药政处处长何毅人。现刊出此次考察报告摘要。
According to the 1985 World Health Organization science and technology exchange program, the Chinese Ministry of Health dispatched pharmaceutical standards and pharmacopoeias inspection teams to visit Britain and Japan from May 11 to June 8, 1986. The purpose of the study is to understand the national drug standards and the organization of Pharmacopoeia and personnel, formulate the procedures and principles of pharmaceutical standards and pharmacopoeia and the examination and approval of new drug quality standards, and draw useful experience to promote the preparation of China’s pharmaceutical standards and pharmacopoeia , Improve the standard level of medicine, and through investigation, establish contact with foreign counterparts and have a large exchange of technical information. The inspection team was led by Deputy Director Jiang Huanbo of the Ministry of Health. Members of the inspection team included Yang Dai, secretary of the Pharmacopoeia Commission, Huang Qiaoshu, director of the Tianjin Drug Control Bureau, and He Yi Ren, director of the Pharmaceutical Administration of the Liaoning Provincial Department of Health. Now published summary report of the inspection.