Dublin, March 25, 2025 (GLOBE NEWSWIRE) -- The "Global Handbook of Medical Devices Regulatory Affairs 2025" directory has been added to ResearchAndMarkets.com's offering. Medical device regulation ...

Evolving regulations and market requirements have kept medtech companies on their toes for years. EU MDR, for example, has ...

The European Society of Cardiology (ESC) has urged the European Commission to revise the Medical Device Regulation (EU ...

In an ever-changing regulatory environment, the role of regulatory affairs personnel is essential to ensure compliance with legislation in all regions in which a company wishes to distribute its drug.

Fellow panellist Pavel Kusnierik, head of regulatory affairs at biotech Contipro ... the overall clinical investigation.” "OCT Medical Devices 2025: biggest regulatory requirement issues ...

Manufacturers are turning to consultancies specialising in medical device regulatory affairs for their UKRP needs, as these can typically grant access to an entire team of specialists and offer ...