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在医药生产过程中,无菌是一个基本条件,为了要提高无菌制剂的水平,则必须要对影响无菌保证水平的因素进行分析,从而确保生产过程中的无菌环境可以得到保证,提高无菌制剂无菌的生产效率。本文对影响无菌保证水平的因素进行探讨,并且提出了控制无菌水平的方法和建议。
Sterility is a basic condition in the pharmaceutical manufacturing process. In order to increase the level of sterile preparations, the factors that affect the level of sterility assurance must be analyzed to ensure that the aseptic environment in the manufacturing process can be guaranteed and improved Sterile preparation aseptic production efficiency. This article explores the factors that affect the level of sterility assurance, and proposes methods and recommendations for controlling sterility levels.