金币
UID225198
帖子
主题
积分1237
注册时间2015-12-18
最后登录1970-1-1
听众
性别保密
|
发表于 2016-8-31 11:22:57
|
显示全部楼层
EU EU Guidelines to GMP, Annex 1: Manufacture of Sterile Medicinal Products (corrected version), 25 November 2008 (rev.)
84. Before any sterilisation process is adopted its suitability for the product and its efficacy in achieving the desired sterilising conditions in all parts of each type of load to be processed should be demonstrated by physical measurements and by biological indicators where appropriate. The validity of the process should be verified at scheduled intervals, at least annually, and whenever significant modifications have been made to the equipment. Records should be kept of the results. |
|