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自《药品管理法》贯彻实施以来,我市中药质量明显提高,1987年检品合格率比1986年同期增长65%.但还存在着一定的问题,假劣药材时有发生,有必要进行分析,找出问题,进一步加强管理,以杜绝假劣药材的发生.一、情况全年检品总数186件,其中送检18件,合格8件.合格率44.4%,不合格10件,不合格率55.6%;抽检168件,合格130件,合格率77.4%,不合格38件,不合格率22.6%.总合格件数138件,合格率74.2%;不合格件数48件,不合格率25.8%.在48件不合格品种中,经营单位44件(占91.7%);使用单位4件(占
Since the implementation of the Drug Administration Law, the quality of Chinese medicine in our city has obviously improved, and the passing rate of seized goods in 1987 increased by 65% compared with the same period of 1986. However, there are still some problems such as the occurrence of counterfeit medicines and the necessity of analysis, Identify the problem and further strengthen the management, in order to eliminate the occurrence of counterfeit and inferior medicine.A total of 186 cases of seized goods throughout the year, of which 18 were submitted for inspection, qualified 8. 44.4% pass rate, failed 10, the failure rate of 55.6 %; Sampling 168, qualified 130, pass rate of 77.4%, 38 failed, 22.6% of the total number of eligible, the passing rate of 74.2%; 48 failed, the rate of 25.8% failed. Among the 48 unqualified varieties, 44 were business units (91.7%), 4 were used units