Clinical trial protocols lay the foundation for R&D, but they aren’t enough to ensure success. People, processes, and ...

Important Note: All IRB protocols for research to be conducted in a foreign country — including survey-only research — must include a completed international research addendum. The international ...

This guidance provides directions for researchers using measures that involve questions related to suicidal ideation. Research shows that asking questions related to suicidal ideation (SI) does not ...

A protocol deviation or violation is any departure from the study procedures or treatment plans as specified in the IRB-approved protocol. Protocol deviations occur when an investigator does not ...

All submissions requiring IACUC review are assigned for review as they are received. Most protocols are reviewed and approved via designated member review (DMR), which allows approval once all review ...

Investigators must use Cayuse to electronically submit new research studies for review and approval, course approvals, continuing research requests, amendments to approved research studies, and ...

If so, then you will need to have your research reviewed by the William & Mary Institutional Review Board (IRB) before you begin your research involving human subjects, so that we're sure that your ...

When discussing the future of clinical trials, people often focus on the promise of exciting new technologies, including artificial intelligence (AI) and predictive modeling. However, even the most ...