The European Union’s transition from the Medical Device Directive to the Medical Device Regulation has overwhelmed orthopedic companies and notified bodies as they seek to interpret and implement the new regulations. With deadlines looming, time is running out for inaction.

Bring your pressing questions to this session to have them answered by an EU MDR expert and former notified body reviewer. Are you unable to get a response from your notified body? Are you seeking clarification on clinical evaluation reports or post-market clinical follow-up reports? Have you experienced successes with the process that you could share with fellow peers? This interactive session provides clarity and solutions for navigating the MDR process.