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为了加强药品不良反应监察报告工作的组织领导、技术复核和情报资料的汇总交流,经研究决定成立卫生部药品不良反应监察中心。该中心办公室设在中国药品生物制品检定所内,不增编制,人员由所内调剂解决,经费在该所年度事业费内调剂,不另增加经费,其主要任务是: 1.根据我部的计划和安排,对我国的药品不良反应监察进行业务技术组织工作; 2.收集、整理、分类、储存与评价来自各地的药品不良反应病例报告资料;
In order to strengthen the organization and leadership of technical supervision and reporting of adverse drug reactions, technical review and the collection and exchange of intelligence information, the research decided to establish the Adverse Drug Reaction Monitoring Center of the Ministry of Health. The main office of the center is located in the China Pharmaceutical and Biological Products Laboratory. The main tasks of the central office are: Arrange and conduct technical and technical work on the surveillance of adverse drug reactions in our country; 2. Collect, sort, sort, store and evaluate case reports of adverse drug reactions from all over the country;