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 ...

As the research coordinator for a large cardiology practice, Sandy Maddock saw the good and the bad ways to conduct clinical trials for medical devices and drugs being developed to help patients.

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.

The CRSP 401 "Introduction to Clinical Research" summer course is designed to familiarize one with the language and concepts of clinical investigation and statistical computing, as well as provide ...