论文部分内容阅读
根据卫生部卫药政(89)第210号文件的通知并受部药政局、医政司的委托,设在中国药品生物制品检定所的卫生部药品不良反应监察中心于1990年4月15~19日在北京举办了药品不良反应监察报告讲习班。部药政局潘学田局长、医政司迟宝兰副司长、解放军总医院医务部杨光承副主任、中国药品生物制品检定所党委书记张
According to the Notice No. 210 of the Ministry of Health Pharmacy (89) and commissioned by the Department of Pharmacy and Medicine and the Department of Medical Affairs, the Adverse Drug Reaction Monitoring Center of the Ministry of Health, China National Institute for the Control of Pharmaceutical and Biological Products, issued on April 15-19, 1990 Japan held a workshop on adverse drug reaction monitoring reports in Beijing. Secretary for Food and Drug Administration Pan Xuetian, Deputy Secretary for Medical Affairs Chi Baolan, Yang Guangcheng, Deputy Director of Medical Department of PLA General Hospital, Party Secretary of China Pharmaceutical and Biological Products Bureau