Resources
FAST-EU: The European Initiative That Could Transform Clinical Trials
Europe has been striving for several years to strengthen its attractiveness as a destination for clinical research. Despite a harmonized regulatory framework established through Regulation
Clinical trials for biotechs: How Europe leverages FDA regulatory instability
The global rollout of clinical trials for biotechs is currently undergoing a massive international regulatory earthquake. Historically, the United States represented the primary, undisputed destination
Decentralized Clinical Trials (DCT): What French Sponsors Still Hesitate to Do
The future of clinical research is increasingly digital, yet France remains cautious when it comes to adopting decentralized clinical trials (DCT). While decentralized clinical trials
Generative AI in medical writing: Revolution or danger zone?
Generative AI in medical writing is now weaving its way into every writing profession. But what happens when the precision of a single word or
Monitoring Visit: Anatomy of a Successful Day for a Clinical Research Associate
A monitoring visit is at the heart of a Clinical Research Associate’s (CRA) role. Between Source Data Verification (SDV), site logistics management, and interactions with
Fake Health Innovations: How to Distinguish Real Innovation from Marketing Hype
The concept of fake health innovations is increasingly discussed in the pharmaceutical, medical device, and digital health sectors. Behind some highly publicized announcements, there may
