随着我国《药品管理法》的颁布和实施，与人民群众的健康密切相关的药品质量问题已引起各级卫生行政部门和医疗单位、药品生产企业的极大关注。《药品管理法》同样对医疗单位配制药品制剂也提出了相应的要求，规定了审批手续、配制条件和制剂的使用范围等，并对制剂的质量检验 With the promulgation and implementation of the “Drug Administration Law” in our country, the quality of medicines closely related to people’s health has drawn great attention from the health administrative departments at all levels, medical units and drug manufacturers. The Drug Administration Law also puts forward corresponding requirements on the preparation of pharmaceutical preparations by medical units, stipulates the examination and approval procedures, the preparation conditions and the application scope of the preparations, etc., and examines the quality of preparations