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.