The MDR Deadline Extension: Use the Time Wisely

Leave a Comment / Class II devices, EU MDR, Focus Article, Medical Device, MedTech, notified bodies, Product Design & Development, Quality/Regulatory, RC - EU MDR and IVDR, RC - Medtech Regulatory Resource Center, state of the art, testing / By

The MDR Deadline Extension: Use the Time Wisely     On March 15, 2023, the European Parliament amended the original Medical Device Regulation (MDR) to lengthen the compliance period for certain medical devices and in vitro diagnostic devices. The move provides device manufacturers with additional time to prepare their products for market and offers a buffer …

The MDR Deadline Extension: Use the Time Wisely Read More »