论文部分内容阅读
卫生部在1986年11月召开的全国药品监督管理工作会议上,对实行产品注册制度提出了明确的要求,并阐明了采取这项措施的重大意义.北京市实施《药品管理法》的试行办法中规定:“药品生产企业生产的药品,要按年度向市卫生局申请登记注册”.北京市卫生局于1987年1月19日发出通知,要求各药品生产企业在规定的期间内进行登记注册,并指出由市药检所具体办理.为了做好此项工作,我们根据市卫生局的指示精神,多次开会研究.我们认为搞好药品
The Ministry of Health held a clear request on the implementation of the product registration system at the national drug regulatory work conference held in November 1986 and clarified the great significance of this measure.The trial implementation of the “Drug Administration Law” in Beijing Stipulates: “Drugs produced by pharmaceutical manufacturers, according to the annual application to the Municipal Health Bureau to register.” Beijing Municipal Health Bureau on January 19, 1987 issued a circular requiring all drug manufacturers to register within the prescribed period , And pointed out that the city drug test by the specific treatment.In order to do this work, according to the instructions of the Municipal Health Bureau, met many times to study.We think that doing a good job of drugs