The success in intra-European healthcare deals requires regulatory expertise, operational flexibility and market-specific ...

Artificial intelligence offers a wide range of opportunities to make medical devices more efficient. How the AI Act and ...

EU member states are set to launch the EU Health Data Space Regulation for harmonised data transfer on 26 March.

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

It’s the start of the new fiscal year here in the UK and it seems like private equity also has tax on its mind.

Marc Pignot, Christian Schübel, Alfred Pauls, Klaas Heinemann discuss their expectations for the new medical device regulations, ahead of the European Parliament's decision this week. On July 10 ...

March 26, 2025, marked a pivotal moment in the EU with the European Health Data Space Regulation, (EU) 2025/327 (“EHDS Regulation”), coming ...

The medical device industry landscape is evolving rapidly, driven both by regulatory changes and the quest for innovation. The new European Medical Device Regulation (EU MDR) and its ...

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

Ministers say they are in the process of determining which of 19 safety systems required for models sold in Europe since last ...

After the European Commission abruptly withdrew its proposal on Standard Essential Patents (SEPs), several MEPs demand explanations. A discussion with Industry Commissioner Séjourné is planned for the ...