Join us for an in-person educational session on the EU AI Act, presented by Jeongpyo (JP) Hong, MS, MPH, Lead Auditor at TÜV SÜD, on Tuesday, November 18, 2025, from 5:00 PM to 7:30 PM Central Time (US & Canada). Learn how this new regulation impacts medical device manufacturers and discover the steps to prepare for compliance.
Thanks to our generous event sponsor, TÜV SÜD, for sharing their facility, knowledge, and providing refreshments for this timely topic!
Are you a student, but not yet a member of the Regulatory Affairs Professional Society (RAPS)? Consider joining today! Otherwise, please reach out to a RAPS Twin Cities Chapter Leadership team member for a discount code to receive complimentary registration.
On-site event at TÜV SÜD America Inc., 141 14th St NW, Saint Paul, Minnesota, USA, 55112-3914
Registration Link:
https://www.raps.org/events/twin-cities-chapter-in-person-event-the-eu-ai-act-what-medical-device-manufacturers-need-to-know
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Georgiann Keyport MSc, RAC, FRAPS
Senior Advisor, Principal Regulatory, Quality and Clinical Affairs Consultant, Adjunct Professor
Canopy Regulatory Solutions Inc.
Chaska MN
United States
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