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I am currently working for a pharmaceutical company that has a document control department and system in place. My background is more ISO 9000/13485 So I have extensive experience with these systems. I can not find any reference to actual control of documents within CFR 21 Part 210 or 211.
Is there any one who can help me with this, people are reciting all sorts of numbers that are guidance for completing, review etc but not control.
thanks
Is there any one who can help me with this, people are reciting all sorts of numbers that are guidance for completing, review etc but not control.
thanks