Mónica Colina

Senior Content Specialist

What Europe’s MDR means for manufacturers of legacy devices

Clarivate regulatory expert  Mónica Colina reviews key aspects of the European Commission’s Medical Device Regulation (MDR) to be considered for surveillance audits of medical devices certified under the repealed directives.  The European Commission’s Medical Device Regulation rules, first published in May 2017, became applicable in all European member states in May of this year. The […]