Complimentary Webinar – February 28, 2018 @ 2pm CET
“AVOIDING THE PITFALLS OF THE NEW CLINICAL DATA REQUIREMENTS UNDER THE MDR”
This webinar will address the new requirements for clinical data under the Medical Device Regulation (EU 2017/745) and propose practical strategies to ensure a smooth transition for manufacturers of devices currently CE marked under the Medical Device Directive (93/42/EEC).
Please register for our event here:
The webinar will be delivered by our Head of Strategic Consulting and VP for Clinical Affairs.