对中药制剂设备清洁验证的探讨

Approach to Depuratory Authentication of Facilities of Chinese Drugs Preparations

目的为中药制剂生产机构的GMP清洁验证工作提供方法和思路。方法分析中药制剂GMP清洁验证工作中清洁规程的优化、可接受标准的确定、检验方法的选择、清洁有效期确定及再验证等方面的特点和难点。结果与结论中药制剂生产设备的清洁规程必须优化。

OBJECTIVE:To provide approaches and avenues for the Chinese drugs preparations manufacturers in the GMP depuratory authentication.METHODS:The features and difficulties in the GMP depuratory authentication of the Chinese drugs preparations such as the optimizing of depuratory regulations,the determination of the acceptable standards,the choice of testing methods,clarification of expiration date and re-authentication were analyzed.RESULT&CONCLUSION:The depuratory regulations of the manufacturing facilities for the Chinese drugs preparations must be optimized.