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21 CFR Part 820 is set regulations issued by FDA which outline how to meet current good manufacturing practices (CGMP) standards for medical device makers within the United States must follow with regards to their quality systems. These CGMP regulations ensure that medical device manufacturers establish an effective QMS to ensure the production of effective, safe and reliable products...Read more at...https://www.i3cglobal.in/fda-qsr-21-cfr-part-820/