- Brexit updates and timelines for CE-marked devices
- Defining new roles of key stakeholders:
- Manufacturer
- Authorized Representative
- Notified Body
- Transition strategies with key action items for planning
- Brexit and the new EU Medical Devices Regulation
Speakers:
Eveline Van Keymeulen
Counsel
Allen & Overy LLP
Jacqueline Bore
Life Sciences PSL
Allen & Overy LLP
Contact:
Brooke Akins | Division Director, Life Science Programs
+1 (312) 224-1693 | bakins@q1productions.com