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Changes to Medical Device Legislation, Adopting ISO 13485 to 21 CFR 820
21 CFR 820 contains the FDA requirements for Quality Management Systems (QMS). These requirements have been established since July 1978.
The FDA has recently amended this regulation to align more closely with QMS requirements used by other global regulatory authorities. The purpose of this presentation is to familiarize attendees with these changes.
Watch this webinar recording to stay ahead of the curve and ensure your Medical Devices QMS meets the latest regulatory standards.
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