(Omnex: Ann Arbor, MI) -- Omnex has announced its latest webinars, “Changes to Medical Device Legislation, Adopting ISO 13485 to 21 CFR 820” and “ASPICE 4.0 is out—are you informed? Hardware point of view”

Webinar: “Changes to Medical Device Legislation, Adopting ISO 13485 to 21 CFR 820”
Date and time: March 28, 2024, 11:00 a.m. Eastern
Speakers: Michael Checketts

21 CFR 820 contains the U.S. Food and Drug Administration 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. Stay ahead of the curve and ensure your QMS meets the latest regulatory standards.

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