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SUMMARY:Sponsored Webcast: Streamlining Multi-Region Submissions: MDR, FDA, and EU AI Act
DESCRIPTION:AI-enabled medical devices must meet overlapping FDA, EU MDR, and EU AI Act requirements. Learn to operationalize compliance with shared data and AI to reduce manual work and accelerate audit-ready submissions.\n
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 Event details: https://www.raps.org/learn-develop/events/sponsored-webcast-streamlining-multi-region-submissions-mdr-fda-and-eu-ai-act.html
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