Human Subjects/IRB
Federal regulations require that all research involving the use of human subjects undergo review by an Institutional Review Board (IRB) to ensure that ethical research is being conducted. ¼ªÏé·»'s IRB, the Committee for Protection of Human Subjects (CPHS), is composed of scientists, non-scientists, and community members with diverse backgrounds to support a comprehensive review of all human subjects research projects. The CPHS is regulated by theÌý, part of the federalÌýDepartment of Health and Human Services.
All researchersÌýand faculty advisorsÌýinvolved in human subjects research must completeÌýHuman Subjects Research trainingÌýthrough the CITI Program.Ìý This training should be completed before beginning a Cayuse application.
¼ªÏé·» uses Cayuse IRB to manage new protocol submissions, renewal applications, modification requests, and protocol deviation or adverse event reporting.ÌýFor more information, see the relevant sections below.Ìý
Note: Student investigators should request Cayuse access usingÌý.Ìý
- Student Researchers
- Review Requirements
- Protocol Submission Process
- Full Committee Dates and Deadlines
- Informed Consent
- Protocol Modifications/Renewals
- Protocol Deviations & Adverse Events
- IRB Class Presentations
- Forms & Policies
- Frequently Asked Questions
- How to Appeal
- Committee
- Recruiting ¼ªÏé·» Students, Faculty, or Staff