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21 CFR Part 11 Guidance for Electronic Records – 2018


: 2018-06-12 : : Informatique médical

Overview:
This includes development of a company philosophy and

approach, and incorporating it into the overall computer system

validation program and plans for individual systems that have this

capability.

Why should you Attend:
This webinar will help you understand in detail the application of

FDA's 21 CFR Part 11 guidance on electronic records/electronic

signatures (ER/ES) for computer systems subject to FDA

regulations. This is critical in order to develop the appropri...

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