IBS:glossary

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FDA 21 CFR Part 820 / Quality System Regulations

Describes current good manufacturing processes for the medical device industry. Intended to ensure that finished devices will be safe and effective for human use. Also known as the Quality System Regulation.
 

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FDA 21 CFR Part 820 / Quality System Regulations

Describes current good manufacturing processes for the medical device industry. Intended to ensure that finished devices will be safe and effective for human use. Also known as the Quality System Regulation.
 

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