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发表于 2017-2-8 23:27:05
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同时我个人觉得所有的复印件使用的文件,表格和模板均应该出自master 文件,表格和模板,这样才是一个industry best practice.下文选自EU GMP
4.2 Documents should be designed, prepared, reviewed, and distributed with care. Theyshould comply with the relevant parts of Product Specification Files, Manufacturing andMarketing Authorisation dossiers, as appropriate. The reproduction of working documentsfrom master documents should not allow any error to be introduced through the reproductionprocess.
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