New European Medical Device and In Vitro Diagnostic Regulations
The European Commission is ushering in a new era of medical device and in vitro diagnostic regulations. What do they mean for industry? Are you ready?
Only RAPS brings together the leading industry experts, regulators and Notified Bodies who have been tracking the evolution of the MDR and IVDR from the beginning. We will connect you with the world’s largest community of regulatory professionals to fully understand the texts and hash out the challenges of tracking and implementing the new requirements. RAPS is here to help you prepare for the changes and understand the impact on your organization’s regulatory resources.
Join our next MDR workshop in Brussels for expert interpretation of new expectations. Be prepared to develop your own transition plans to navigate market access (CE Marking) expectations for both new and legacy devices being placed in Europe.
Transitioning to the new EU MDR and IVDR: A Workshop on Real World Implementation Experiences