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 ...

Knowing whether or not a treatment is working just by wearing your watch? Data scientist Ahnjili ZhuParris has identified a lot of opportunities for the use of machine learning in clinical research to ...

Over the last 10 years, clinical trials have changed substantially in response to increasing globalization and study complexity, along with new technological capabilities and industry guidelines 7.

MORRISVILLE, N.C.--(BUSINESS WIRE)--PharmAlliance, a diversified pharmaceutical and life sciences services provider, is pleased to announce its acquisition of Monitorforhire (MFH), a robust business ...

As part of the quality assurance process to ensure the integrity of the trial data at the site, clinical trial monitors for both Sponsors and CROs can access participants’ electronic health records at ...

Clinical trials can vary in length depending on several factors. Here's what you need to know about how long clinical trials ...

Venetoclax is the standard of care for chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) but requires intensive monitoring for optimal safety. Clinical relevance of intensive ...

There are several start-up fees when you initiate a clinical trial. These vary depending on the design of the study. Below, we have defined the fees and identifed the responsible parties. This fee ...