Date: Thursday 6 July 2023
Time: 17.00 - 19.00 (Registration for 16.30)
Followed by a drinks reception
The Medical Devices Regulations are a fundamental change to the regulation of higher risk medical devices in Europe, imposing far more prescriptive and onerous obligations on industry, regulators and notified bodies than previously.
A panel of regulatory experts chaired by John Wilkinson will discuss the implications, direct and indirect, of the regulations on the EU and British medical devices industries, regulators and notified bodies. Then a panel of EU and UK lawyers will consider the implications for products and related litigation. The mix of the regulatory and litigation views will give valuable insights to this important topic.
John Wilkinson, Cooley LLP
- Graeme Tunbridge, Senior Vice President Medical Devices, BSI
- Roddy Bourke, McCann FitzGerald LLP
- Sarah Moore, Hausfeld LLP
- Jantina Hiemstra, Hausfeld LLP
- Dr Peter Feldschreiber, Clerksroom
- Aline Lautenberg, Director Legal & Compliance, MedTech Europe
- Dr Tom Melvin, Trinity College Dublin
Event convened by Duncan Fairgrieve, Senior Research Fellow in Comparative Law and Director of the Product Liability Forum, BIICL
This event offers the equivalent of 2 CPD hours.
If you have any queries, please contact the Events team.
Please note that our events may be photographed or recorded. These materials will be used for internal and external promotional purposes only by the British Institute of International and Comparative Law. If you object to appearing in recordings or photographs, please contact the Events team to let us know ahead of the event.
Event Cancellation Policy
When you register for an event you will be asked to confirm that you have read and understood our cancellation policy.