Faculty Fellows Program Background and Objectives Faculty experience multiple obligations in teaching, research, and mentoring. Large proposals require a significant investment of time and resources, including but not limited to:... Read More

Federal regulations, state laws and University policies recognize that researchers may have financial interests in research sponsors and/or in entities with business interests closely related to their research. The term... Read More

Responsibilities apply to faculty supervising students/medical residents as a Principal Investigator (PI). The IRB holds the Faculty Advisor(s) responsible for the overall management of an approved research protocol in conjunction... Read More

The IRB has three full board committees that review all human subject research studies that are considered greater than minimal risk to the subjects. There are two biomedical/clinical committees one... Read More

Investigators are required to report certain events that occur during the conduct of a study to the UC Davis IRB. These events are referred to as reportable events. The terms... Read More

All researchers should be conducting their IRB approved protocols in accordance with requirements in the Investigator Manual. This document is designed to guide you through policies and procedures related to... Read More

All human subjects research projects require IRB review, regardless of funding. To determine if a project requires submission to the IRB, you must assess two criteria: Is this project research?... Read More

  Subscribe to the IRB-Info Listserv to stay informed of changes to the UC Davis IRB Administration Website and/or policy and procedure changes of the UC Davis Institutional Review Board... Read More

This page is designed to provide an overview of the IRB reliance agreement process at UC Davis. If you need additional information, please contact the Reliance Team for assistance. In... Read More