Two EU Notified Body Frontrunners In Race For Designation Under New Regulations

The European Union’s new Medical Device Regulations call for the naming of notified bodies for medtech testing and certification, and two as-yet unnamed organizations are at the forefront as contenders for these coveted positions. Device companies are eagerly awaiting the announcement and see it as the first step in gaining a competitive advantage on the marketplace by gaining a CE-number. Dive into more details surrounding the notified bodies designation in this insightful article from Medtech Insight.