AI’s reach depends on the environments in which it operates as well as how it is developed and deployed, highlighting a ...

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 ...

Switzerland is working toward reestablishing its relationship with the EU while exploring new avenues. Meanwhile, the U.K. is ...

While recent draft guidance from the Food and Drug Administration pertaining to artificial intelligence-enable medical ...

The International Directory of Medical Devices & Diagnostics Companies 2025 profiles over 6,000 companies and 8,000 key executives across the globe.

The integration of AI and cloud technologies is transforming pharmaceutical manufacturing regulations, focusing on safety, efficiency, and global harmonization.

Tevogen Bio is driven by a team of highly experienced industry leaders and distinguished scientists with drug development and ...

The Global Handbook of Medical Devices Regulatory Affairs 2025 provides comprehensive, country-by-country insights into medical device regulations worldwide. Covering 70+ countries, it includes ...