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This virtual webcast examines revisions to Annex VII of Regulation (EU) 2017/745 and their implications for notified bodies and medical device manufacturers. Participants will learn about changes affecting notified body competencies, conformity assessment procedures, certification timelines, and strategies for maintaining regulatory readiness.
Date
Time
09:00 AMPlatform
Digital Hub
Global
Hosted By
Regulatory Affairs Professionals Society (RAPS)
All times are in Africa/Casablanca.
Presentation addressing revised Annex VII requirements and practical implications for manufacturers and notified bodies.
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