Medical Device and In Vitro Diagnostic Regulations are changing. How will you be affected?

Listen as Ben Jacoby, Regulatory Expert, talks with Adrian Dawkes about the transition to the new regulations in Europe and UK:

• Can existing products continue to be sold?
• What will global manufacturers need to do?
• What is the impact for companion diagnostics being used alongside drugs in clinical trials?
• How is the environment in Great Britain different, and what does this mean for innovators?
• What’s the impact for patients?

A rare opportunity to hear from one of the most experienced regulatory advisors in this important space.