businessHosted by Regulatory Affairs Professionals Society (RAPS)

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This free online webcast explores the application of artificial intelligence to Clinical Evaluation Report workflows under the EU MDR. Experts will discuss improving clinical evidence traceability, regulatory documentation efficiency, consistency, notified body readiness, and maintaining human oversight in AI-assisted regulatory activities.
Date
Time
09:00 AMPlatform
Digital Hub
Global
Hosted By
Regulatory Affairs Professionals Society (RAPS)
Dawn (Kellogg) Merriman, PhD
Regulatory Affairs Manager, Hologic
Shruti Sharma
AI Product Specialist, Celegence
All times are in Africa/Casablanca.
Discussion of AI-supported clinical evaluation workflows, evidence management, traceability, regulatory defensibility and notified body readiness.
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