Changes to Medical Device Legislation, Adopting ISO 13485 to 21 CFR 820 | Michael B. Checketts 

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Michael Checketts, a medical device industry veteran, joined us on a webinar on the latest changes to medical device legislation, focusing on the adoption of ISO 13485:2016 and updates to 21 CFR Part 820, and provided practical insights on how these changes impact quality management systems, labeling, packaging controls, and compliance requirements.
Watch the full session to gain valuable insights!