在医院制剂工作中,进行注射液的澄明度检查时,常常需对澄明度检查的不合格品分类登记。分类登记不仅可保障制剂产品的质量,而且可以针对澄明度不合格的性质,找出生产中相应的薄弱环节,采取有效措施,提高澄明度合格率。如“纤维”类较多,则应改穿绸质或化纤工作服,提高灌装室空气净化的程度;“白点”类较多,则应检查终端微孔滤膜是否 In the hospital preparations, the clarity of the injection test, often need to check the clarity of non-conforming products classified registration. Classification registration can not only guarantee the quality of preparation products, but also can find out the corresponding weak links in the production according to the unqualified clarity, and take effective measures to improve the passing rate of clarity. Such as “fiber ” category is more, you should change through the silk or chemical fiber uniforms to improve the degree of filling room air purification; “white spots ” category is more, you should check whether the terminal microporous membrane