GMP Regulation Handbook: Medical Devices, 21 CFR Part 820

Medical Devices and in Vitro Diagnostics Products 21 CFR Part 820

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GMP Regulation Handbook: Medical Devices, 21 CFR Part 820

Regulation Handbook: 21 CFR Part 820: Medical Devices
Quality Systems Regulation (formerly known as Current Good Manufacturing Practice for Medical Devices and in Vitro Diagnostics Products)

Revisions as of April 2017