六月 10, 2024 - 六月 14, 2024
Date: 10 - 14 June, 2024
Location: DoubleTree by Hilton Brussels City, Brussels, Belgium (Hybrid Event)
The flagship regulatory event for the medical device and in vitro diagnostic industry promises an immersive experience, delving into eight cutting-edge topic streams that encapsulate the industry's most pressing concerns. Covering EU MDR/IVDR, Clinical Investigations, Post-Market Surveillance, Software/AI, Biocompatibility, Law & Compliance, and Global Market Access, this event serves as a comprehensive platform for professionals seeking to navigate the complex regulatory landscape.
Participants can anticipate gaining critical insights directly from authoritative figures, including representatives from the EU Commission, Competent Authority, Notified Body, and industry pioneers within the medical device and IVD sectors. This unique convergence of expertise ensures a rich and enlightening exploration of the challenges and opportunities shaping the future of regulatory compliance in the healthcare sector.
Join Gert Bos during the event for the following sessions:
- June 10th, 8:40-9:40am CET, EU MDR: Timelines, Transitions and Tribulations
- June 11th, 16:45-17:45 CET, EU MDR Open Forum: Ask the Experts
- June 13th, 16:45-17:45 CET, Planning the Perfect Post Market Clinical Follow-Up (PMCF) & Post Market Performance Follow-Up (PMPF).
As a hybrid event, delegates will have the option to attend either in-person or digitally.
For more information about the event and to order tickets, please visit the MedTech Summit website.