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我们在依据《中国药典》1990年版一部制剂通则和凡例的规定制订企业具体品种、规格的质量标准中发现尚有不妥之处,给制定标准带来实际的困难。为此,列举以下几点,供同道讨论及药典修定时
We found that there are still some defects in the formulation of the quality standards for the specific products and specifications of enterprises according to the General Rules for Pharmaceutical Preparations of the 1990 edition of the Chinese Pharmacopoeia. To this end, the following points are listed for discussion and pharmacopoeia revision