EU moves to fix failing medical and in vitro device rules and spur innovation
Shorouk Express A ‘targeted’ revision to the MDR and IVDR promises clearer timelines, proportionate oversight and faster access to innovative technologies. The European Commission has unveiled its long-awaited targeted revision of the EU Medical Devices Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), aiming to ease the regulatory burden on manufacturers, while ensuring Europe’s high…
