论文部分内容阅读
为了配合《新药审批办法》有关中药部分的修订和补充规定(1992年9月1日起)的执行,进一步完善中药新药的审批管理,促进中药新药研制的发展,1992年6月29日至7月16日,由卫生部药政局主办的中药新药研讨班在北京举行,来自全国省级的药政、药检部门和部分药厂的同志参加了这次研讨班。栗福民、杨拾宁等卫生部药政局有关领
In order to comply with the implementation of the provisions of the Measures for the Examination and Approval of New Drugs concerning the revision and supplementation of the Chinese medicine (from September 1, 1992), further improve the examination and approval of the administration of new Chinese medicines and promote the development of new drug research for traditional Chinese medicines. From June 29 to June 7, 1992 On January 16, a symposium on traditional Chinese medicine and new drugs sponsored by the Pharmaceutical Affairs Bureau of the Ministry of Health was held in Beijing. Comrades from the provincial pharmaceutical administrations, drug inspection departments and some pharmaceutical companies attended the seminar. Li Fumin, Yang Shining and other relevant departments of the Ministry of Health Drug Administration