MedTech Europe’s report reflects a lack of clarity over requirements, rising costs, and decreases in innovation activities.

Stakeholders branded the MDR and IVDR rules “unreasonably complicated,” “terrible for EU patients and doctors” and “a mess.” ...

In recent years, new regulation has been top-of-mind for medtech companies wishing to continue marketing their products in ...

New European Union rules for health technology assessments become effective: Amsterdam, The Netherlands Monday, January 13, 2025, 10:00 Hrs [IST] EMA is ready to support the imple ...

A European Union probe into China’s procurement of medical devices confirmed the bloc’s concerns that the Asian country ...

The European Commission said on Tuesday it had found "clear evidence" that EU suppliers of medical devices are not given fair ...

The European Commission has presented a new action plan to enhance the cybersecurity of the healthcare sector amid a rise in ...

An EU investigation has found discrimination against European companies in China's public procurement market for medical ...

Medtronic (MDT) announced CE Mark approval in the European Union and the United Kingdom for BrainSense Adaptive deep brain stimulation and ...

Artificial intelligence (AI) is transforming the health care landscape, from diagnostics to drug development and clinical trials. As AI ...