21 CFR Part 820 (Medical Device QSR) - Practice Exam

21 CFR Part 820 - Quality System Regulation is the set of regulatory requirements on Quality System for medical devices manufacturers in the U. S. A.

The regulation is not only applied in the U. S. but also many other countries have taken inspiration from it for making their own regulations or adopting it as a guidance.

It is one of the important regulatory document on medical device manufacturer's Quality System. If you are a quality or regulatory professional or beginner in the medical devices industry, you should check your expertise in Quality System Regulation (QSR). This "knowledge validation exam" helps you to check and validate your knowledge on 21 CFR Part 820 regulation and its fundamental concepts.

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