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1987年我局在执行《药品管理法》,加强药品监督管理方面做了一系列工作,现简述如下.一、继续抓了《药品管理法》的宣传1987年我局有针对性地系统讲解《药品管理法》,阐述了合法与非法,守法与违法的界限.同时印发了药政药检通讯和药政法规汇编两万余册,向广大医药人员提供了学习资料.对药品监督管理执法中不甚明确和一些具体的问题及时发文件进行说明和作出补充规定,如医疗单位委托药厂加工制剂应向市,区(县)卫生局备案,有的单位因不明确而未照办,我
In 1987, our bureau made a series of work in the implementation of the “Drug Administration Law” and the supervision and administration of drugs, which are summarized as follows: 1. Continue to catch the propaganda of the “Drug Administration Law” In 1987, I deliberately explained the system The Drug Administration Law sets forth the boundaries between lawfulness and illegality, law-abiding and law-breaking, and has published over 20,000 copies of the Pharmaceutical and Drug Administration Newsletters and the Pharmaceutical and Pharmaceutical Regulations to provide learning materials to the general medical staff. Not clear and some specific issues in time to send documents to explain and make additional provisions, such as medical units commissioned by the pharmaceutical processing company should be to the city, district (county) Health Bureau for the record, some units because of ambiguity did not do, I