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Home › 21 CFR Part 11 Industry Overview: Ready For An FDA Inspection?

 

21 CFR Part 11 Industry Overview: Ready For An FDA Inspection?

2013-09-05 03:02:29| drugdiscoveryonline Downloads

The U.S. Food and Drug Administration (FDA) issued 21 CFR Part 11 in 1997 to establish criteria for the use of electronic records andelectronic signatures by organizations that comply with the federal Food, Drug, and Cosmetic Act and the Public Health Service Act.

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Category:Biotechnology and Pharmaceuticals

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