businessHosted by Regulatory Affairs Professionals Society (RAPS)

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.
Explore other relevant upcoming events.

The European Conference on Digital Transformation & Data in Medical Technologies (DTD2026) will take place on 26–27 October 2026 in Munich, Germany, bringing together MedTech industry leade...

The 5th TEAM-PRRC Annual Summit is a European event dedicated to Persons Responsible for Regulatory Compliance (PRRCs), regulatory affairs and quality professionals in the medical device se...

Veeva MedTech Summit Europe brings together medical technology leaders for more than 40 educational sessions across regulatory, quality, clinical, commercial, technology and medical affairs...

The RAPS AI in Regulatory Conference explores how artificial intelligence is transforming regulatory affairs across the healthcare product lifecycle. The program focuses on practical AI app...