IRB Operations
The Institutional Review Board consists of independent committees established to advocate for the protection of the rights and welfare of human participants involved in research. The IRBs evaluate proposals for new research and conduct reviews of on-going research following Guiding Ethical Principles and federal and institutional requirements for the protection of human subjects.
IRB Membership
- IRB Assurance and Membership Representation Statement
- IRB Membership Information
- Application for IRB Membership
- IRB Member Annual Agreement
IRB Meetings and Reviewer Checklists
- IRB Meeting and Room Schedule 2013
Checklists:
- Initial Review (Convened Board)
- Exempt and Expedited Categories Chart
- Expedited Review
- Exempt Determination
- Modification Review Form
- Modification Expedited Review Form
- Protocol Exception Review Form
- Unanticipated Problem Report Review Form Guidance
- Continuation Review Summation (Form sent in IRB packet with pre-review notes)
- Humanitarian Use Device (HUD) Review Form Guidance
- Emergency Use of a Test Article
IRB Policies and Guidance
- IRB Policies and Procedures
- The Belmont Report
- Regulatory Links
- IRB Reference Booklet
- Glossary of Terms
- Guidelines for IRB Review
- IRB Review Criteria
- Expedited and Exempt Categories
- Determining Substantive Vs Minor Changes in Research
- Assessing the Need for Certificates of Confidentiality (CoC)
- Drug Information Resources - Internal links only
- Lexi-Comp Online - uses, warnings, adverse events, drug interactions, etc.
- Micromedex - summary, DrugDex detail, package inserts, etc.
- Pharmacy webpage - Management of Investigational Drugs - Policy 1405 PAM