New Medical Device Regulation (Mar, 2019)

New Medical Device Regulation is organized by Management Forum (Mf) Ltd and will be held from Mar 06 - 07, 2019 at The Rembrandt Hotel, London, England, United Kingdom.

The target audience for this medical event is Regulatory affairs, Clinical studies, Vigilance PMS, Quality systems Technical support and business development.

Course Overview:
The New Medical Device Regulation (MDR) brings about a period of great change, uncertainty, and opportunity within the medical technology and diagnostics sectors. This seminar will help you embrace these changes and operate successfully in the new environment in Europe. It will cover in depth the new regulations and their implementation by the Member States and Notified Bodies. You will get to hear the latest thoughts on clinical development, safety monitoring and the implications of Brexit.

Why you should attend
This seminar will provide key guidance and interpretation of the changes to the regulation and will be of value to all those who are involved in placing a medical device on the market, and anyone who requires an essential overview of the new medical device regulation and its impact on the industry and working practices.

Benefits of attending:
• Hear from key opinion leaders regarding the impact of the changes
• Get an essential understanding of the new regulation
• Be aware of how the changes will be implemented by Member States and Notified Bodies
• Plan how to manage the transition successfully
• Understand how to comply with the new regulations
• Discuss the implications of Brexit

Tickets :
Early Fee (Before Dec 21, 2018): €2182.80
Late Fee (After Dec 21, 2018): €2518.80
Multiple booking discount for 2nd or subsequent delegates: €2140.98

Early Fee (Before Dec 21, 2018): USD 2,026.00 (+ Vat)
Late Fee (After Dec 21, 2018): USD 2,338.00 (+ Vat)

Additional details will be posted as soon as they are available.