JOIN NOW FOR THE PRE-CONFERENCE WORKSHOP!
(limited places available)

Join us for this highly interactive workshop featuring hands-on sessions.
Delegates will explore strategies and discuss potential pitfalls and solutions in four streams:

• New Product Development
• Clinical evidence strategies for market approval
• Post Market Surveillance, reporting and risk management
• Evidence generation through Post Market Clinical Follow Up studies

Target Audience:  Regulatory and Clinical Leaders and Decision Makers in the Medical Device and IVD Industry.
Venue: Hilton London Canary Wharf

To View the Pre-Conference Workshop Programme:  CLICK HERE

Pre-Conference Workshop Chair

Dr. Amie Smirthwaite PhD, FRAPS
Senior Vice President, Scientific Affairs
RQM+, UK