Necessary Steps: Achieving FDA 21 CFR Part 820 Compliance For Medical Device Manufacturers
In the world of manufacturing medical devices, compliance to FDA regulations is crucial. The FDA 21 CFR part 820 (also known as the Quality System Regulation) outlines the current Good Manufacturing Practices (CGMP) for the design and manufacturing of medical devices. The FDA 21 CFR Part 820, referred to as the Quality System Regulation provides […]