Getting ready for Europe’s new MDR - Clinical Evaluation
The European medical regulatory landscape is undergoing its most significant overhaul in years. The eagerly-awaited Medical Device Regulation (MDR), expected to be published in Q2 2017, will bring substantial changes to the way medical device manufacturers bring their devices into the European market.
At the heart of the current Medical Device Directive review lies the subject of the clinical evaluation.
This white paper guides you through nine important factors for the successful planning, development and maintenance of a Clinical Evaluation Report (CER). Download your FREE paper below.