作为药品生产单位，无菌注射剂生产中污染的控制及无菌检查直接影响到无菌产品的微生物方面的质量控制。
As to be the drag manufacturer, it will directly influence the biological quality control of sterility product that the contaminations control during injection production and sterility test.
目的探讨薄膜过滤法在小容量注射剂无菌检查中应用的可行性。
Objective:To determine the validity of membrane filtration method in the sterility test of little capacity injection.
应用推荐