Eight years since the EU’s Medical Devices Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR) entered into force, progress has been made, but major challenges remain. Europe’s medical technology regulatory system is still unpredictable, costly and slow in bringing innovation to patients (see MedTech Europe’s 2024 survey ➡️ https://bit.ly/4gKo2u5)
MedTech Europe has recently published a new leaflet outlining four urgent targeted measures to restore the system’s functionality ahead of a full reform planned after the European Commission’s targeted evaluation.
Download the leaflet here ➡️ https://bit.ly/4keRk5Q
Visit our Future of Regulatory System webpage here to learn more. ➡️ https://bit.ly/3Y0eiV7
