Breakfast Meeting – Preparing for MDR
8:00-11:00, Wednesday 18th April 2018 (Room W1)
Join us for a Regulatory Workshop on the second day of Medtec Europe. This session is free to attend and will provide in-depth insights into the interpretation and application of the new EU MDR ahead of the 2019 deadline.This meeting will cover perspectives from regulatory, industry and consultancy representatives, providing tangible advice on interpreting, preparing for and implementing the new regulations.
Free to attend, advance registration required.
In collaboration with TÜV SÜD Product Service.
REGISTRATION OPENING SOON
8:00-8:30 Breakfast and Networking
8:30-9:15 The Notified Bodies Perspective: Expectations from Industry
Martin Witte, Global Director Active Medical Implants, TÜV SÜD Product Service (confirmed)
9:15-10:00 Industry Case Study: EU MDR, what has been the earl experience and lessons learned?
10:00-10:45 Why start now: A practical approach to kick-starting your MDR/ IVDR implementation
Jay Crowley, Vice President of the Unique Device Identification Services and Solutions, USDM Life Sciences (confirmed)
10:45-11:00 Coffee & Networking
Close of event