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为了进一步贯彻《药品管理法》,提高药品质量,保证人民用药安全有效,我们对本市生产,经营和医疗单位的中成药进行了抽验,并将1986～1990年抽验结果分析如下。 一、基本情况 五年内,我们着重对质量有问题的品种进行了抽验。抽验170个品种,计774批,按《中国药典》,部颁药品标准、地方标准及医院制剂规范进行了检验,并将五年内抽验的中成药质量情况做了比较和分析(表1、2、3)。
In order to further implement the “Drug Administration Law”, improve the quality of medicines and ensure the safety and effectiveness of drug use by the people, we conducted random tests on proprietary Chinese medicines in the production, operation and medical units of the municipality and analyzed the results from 1986 to 1990 as follows. First, the basic situation Within five years, we focused on quality problems have been tested. A total of 170 varieties were tested and 774 batches were tested. The tests were conducted according to the standards of Chinese Pharmacopoeia, ministerial pharmaceutical standards, local standards and hospital preparation specifications. The quality of Chinese patent medicines sampled in five years was compared and analyzed (Tables 1 and 2 , 3).