Discussions on the EU Medical Device Regulation will be reaching their conclusion over the next few months and the legislators (European Commission, Parliament and Council of Ministers) will negotiate on its final form during the autumn. This year’s Regulatory Conference will provide delegates with a comprehensive update on the very latest developments in the legislative process which is currently taking place in Brussels. It is anticipated that by September the final shape of the new Regulation will be sufficiently discernible as to enable manufacturers, importers and distributors to start planning for implementation.

If you want to know how the this new and important framework is likely to affect your business or healthcare institution then this event is not to be missed. With strong and informative speakers from across the regulatory community, the conference will provide authoritative views on how the new legislation will affect your business in the future.

Topics to be covered

• Current Overview –  the Regulators and Industry
• MHRA Policy Developments
• The Hot Topics – Industry Experts
• International Regulatory Developments

Confirmed Speakers

• Graeme Tunbridge, Head of Medical Devices EU Policy, MHRA
• John Brennan, Director Regulations and Industrial Policy, Eucomed
• Dr Neil Adams, Director, Healthcare Operations and Delivery, BSI
• Martin Penver, Head of Notified Body – Medical Directives, LRQA
• John Wilkinson OBE, Director of Devices MHRA
• Peter Schroeer, Group Director EMEA Regulatory Affairs, Global Surgery Group, Ethicon Endo-Surgery (Europe) GmbH
• Nigel Talboys, Director Government Affairs & Public Policy EMEA, Terumo BCT

Contacts

Liz Hatter
Events and International Manager
0207 960 4368

Jane Sessenwein
Events and International Manager
0207 960 4380

View more here