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