FDA’s Proposed Changes to 21 CFR 820 | Michael B. Checketts

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you involved in the medical device industry or interested in FDA regulations? The FDA has proposed significant changes to 21 CFR 820, which governs quality management systems for medical devices. In this video, we break down the key modifications proposed by the FDA, discussing their potential impact on manufacturers, compliance requirements, and overall industry landscape. Stay informed and prepared for the future of medical device regulation by watching this informative video.