CLINICAL EVALUATION OF MEDICAL DEVICE NEW RULES WITH MDR

I3c Global24 Nov, 2022Business

The new EU regulation on medical devices (MDR) has already entered into force. They establish a modern and stronger regulatory framework to protect public health and patient safety. The new rules start to apply after a one-year postponement due to the coronavirus pandemic, addressing the need for greater availability of vitally important medical devices or MDR Clinical Evaluation Report across the EU.