Updating monitoring strategies and combining them with the latest technology can streamline clinical trial processes to generate higher quality data and increase patient safety, says Brett Wilson.

Sponsors of clinical trials in the United States have a regulatory responsibility under 21 CFR Part 312.50 to monitor the progress of clinical studies. Historically, Sponsors performed in-person ...

This post is sponsored by IMARC Research, Inc. In the realm of clinical research, two functions often work together to complement each other to create an additive impact on the overall quality and ...

Clinical trials, often one of the most expensive parts of bringing a drug to market, can last as long as a decade. The Covid-19 pandemic has proven clinical trials can be successfully completed in ...

In May 2026, the 4th AGP & DTx Summit concluded successfully in Shenzhen under the theme 'Beyond Glucose.' With SIBIONICS serving as a co-organizer, the summit brought together international experts, ...

Veterinary algorithms build individual baselines to detect subtle shifts in a pet's health and therapy response.