Registration at full capacity.
We do encourage you to register for our Virtual Program: Key Challenges in Preparing for EU Medical Device Regulation (MDR)
RAPS is joining forces with fellow member organization TOPRA to deliver a first of its kind workshop that covers everything you need to know about MDR and 'combination' products. We are bringing together representatives of the European Commission, Member State medicinal and medical device authorities, Notified Bodies and industry experts to explore the complex issue of MDR.
This workshop will include a full review of the changes MDR will bring and explore the impact of the MDR on:
- Medical devices incorporating ancillary medicinal substances/human blood products
- Medicinal products incorporating medical devices as single integral products
Don't miss your chance to have your say!