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各省、自治区、直辖市卫生厅(局): 根据《药品管理法》和《药品管理法实施办法》关于药品生产、经营企业和医疗单位制剂《许可证》期限的规定,从1990年元月起,对全国所有药品生产,经营企业和医疗单位制剂室进行审核、换发《许可证》,有关事项已以卫药字(89)第39号和卫药政字(90)第38号文通知各地。目前,各地正在组织对药品生产,经营企业和医疗单位制剂室的验收,有的省已完成了第一批、第二批的验收计划。
Health Bureau (bureau) of each province, autonomous region and municipality directly under the Central Government: In accordance with the provisions of the “Drug Administration Law” and the “Implementation Measures of the Drug Administration Law” on the “license” period for the preparation of pharmaceutical products, business enterprises and medical units, starting from January 1990, All the country’s pharmaceutical production and management enterprises and medical units of the preparation room for review, renewal of the “permit”, the matter has been Senate word (89) No. 39 and Weiyaozhengzi (90) No. 38 to inform around . At present, all parts of the country are organizing the acceptance of pharmaceutical preparation and distribution enterprises and medical units. Some provinces have already completed the first and second batch of acceptance plans.