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Medical Devices

QS Regulation 6: Acceptance Activities; Nonconforming Product

About the Course

The sixth in a series of Quality System (QS) Regulation employee training courses discusses Acceptance Activities (21 CFR Part 820 Subpart H) and Nonconforming Product (21 CFR Part 820 Subpart I). The QS Regulation provides a framework of basic requirements for manufacturers of finished medical devices