🚀 Join Regulatory Affairs Professionals Society (RAPS) and the RAPS Twin Cities Chapter for an exciting opportunity to learn about the latest developments in Post-Market Surveillance Activities for Medical Devices in the European Union!
🗓️ This in-person event will be held on Thursday, June 12, 2025 from 5:00 pm - 7:30 pm at the New Brighton, MN facility of TÜV SÜD, one of the leading Notified Bodies!!
🧠 Learn from Adam True, current Relationship Manager with TÜV SÜD and experienced Lead Auditor!
Join TÜV SÜD and RAPS for an exclusive in-person event focused on demystifying Post-Market Surveillance (PMS) activities under the European Union Medical Device Regulation (EU MDR). Designed for medical device manufacturers navigating the complexities of post-market obligations, this session will address frequently asked questions, clarify regulatory requirements, and provide best practices to support ongoing compliance and patient safety.
🏢 Before the educational session begins, attendees are invited to network and participate in an optional guided tour of TÜV SÜD's Medical Device Testing Center of Excellence in New Brighton, Minnesota - one of North American's most comprehensive medical device testing facilities. (Please note: to protect proprietary information, direct competitors of TÜV SÜD will not be permitted to join the lab tours.)
Agenda:
- 5:00 - 6:00 PM Registration, Networking, Light Food, and Optional Lab Tours
- 6:00 - 6:45 PM Educational session with Adam True (overview of EU MDR PMS requirements, compliance processes, and best practices)
- 6:45 - 7:15 PM Audience Q&A
- 7:15 - 7:30 PM Closing Remarks
✏️ Space is limited. Register today at: Twin Cities Chapter In Person Event: EU MDR Post-Market Surveillance Activities - Frequently Asked Questions
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| Twin Cities Chapter In Person Event: EU MDR Post-Market Surveillance Activities - Frequently Asked Questions |
| Join TÜV SÜD to explore the intricacies of post-market surveillance (PMS) under EU MDR. We'll cover common questions, compliance requirements, and best practices to help ensure the safety and performance of your medical devices. |
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Lisa Pritchard
VP of Regulatory, Quality, Clinical and Engineering
DuVal & Associates PA
Bloomington MN
United States
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