This is the 21 CFR Part 820 Quality System Regulation document. Now you have it at your finger tips. A must have for any medical device manufacturer. Use it at your own risk and ensure that revision is current before use.
This is the 21 CFR Part 820 Quality System Regulation document. Now you have it at your finger tips. A must have for any medical device manufacturer. Use it at your own risk and ensure that revision is current before use.