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发表于 2021-2-15 14:21:48
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10.6 Data Integrity Issues with Paper Records
The current situation in many GMP laboratories is that many are paper based and working practices have hardly changed over last 2–3 decades. In fact,the FDA Guide to Inspection of Pharmaceutical Quality Control Laboratories issued in 1993 is still relevant a quarter of a century after publication as many working practices have not changed. The key issue is one of the master templates and blank paper forms.
Do not take from me that blank forms are a high regulatory risk, here is the FDA perspective on the problems with blank forms with two regulatory citations from warning letters.
Facta Farmaceutici S.p.A., FDA Warning Letter, January 2017 (ref. 9) Citation 2 states:
原文在这里,感兴趣可以自己看第十章,我应该没玩错。 |
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