Regulatory check-up: 1 hour free consultancy

This offer is available every second Tuesday of a month

Since May 2021, the new EU Medical Devices Regulation ((EU) 2017/745 Regulation on medical devices (MDR)) has come into force, and from May 2022, the new EU In-vitro Diagnostics Regulation ((EU) 2017/746 Regulation on in-vitro diagnostic medical devices (IVDR)) will follow it. This will be accompanied by far-reaching changes, including in the classification, clinical testing, and quality management of medical devices and in-vitro diagnostics.