The FDA 21 CFR PART 820: Medical Devices Quality System Regulation (QSR)

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The FDA 21 CFR PART 820: Medical Devices Quality System Regulation (QSR)

Determining and setting up a quality system is a challenging task for medical devices manufacturers. A robust quality system covers the aspects like the medical device design, manufacturing, supplier management, product labeling, storage & distribution, clinical data, risk management and complaint handling. The US FDA maintains a Quality System Regulation (QSR), which ensures that all the medical devices sold in the USA are safe, quality-oriented and effective for their intended use.