Implications for Medtech Companies with FDA Rollout of the New QMSR to Replace Current QSR

Taking Advantage of the EU MDR Delay in Uncertain Times – Webinar

How to Start Preparing Your Team for the EUDAMED Database – Webinar

Clinical Evaluations for Unique Product Types Under the EU MDR – Webinar

Best Practices for UDI Implementation and EUDAMED Submissions – Webinar

Combination Products: Seeking a Notified Body Opinion According to MDR Article 117

Medical Device Virtual Summit – Morning Program

Medical Device Virtual Summit – Afternoon Program

The Ins and Outs of Post Market Surveillance Under the EU MDR