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本文从药材的加工炮制、制剂的工艺过程和有关成分的监控,较全面地论述了中药制剂质量标准制定的方法和要求,对药厂研制部门制定质量标准有一定的参考价值。
This article discusses the methods and requirements for the preparation of quality standards for Chinese medicine preparations from the processing and processing of medicinal materials, the process of preparations, and the monitoring of related ingredients. It has certain reference value for the development of quality standards for pharmaceutical research and development departments.