II. IRB Forms
Please Note: Application forms are updated one or more times a year to improve the review of research and protection of human subjects. You must use the most current version of forms on this site when you are submitting research for review.
New Project Applications
- IRB Research Application
- QA/QI Application
- Grant Review Application & Instructions
- Specimen/Data Repository Application
- Humanitarian Use Device Application
- Non-Human Subjects Determination Application
- International Research Application added 5/8/2012
Annual Review, Changes and Updates
- Continuing Review Application (Use for annual review and/or study conclusions)
- Change / Update Form (Use for amendments, study status changes, personnel updates, etc.)
- Conclusion Form
Reports to the IRB
- Protocol Violation Form updated 1/20/2012
- Research Financial Disclosure Questionnaire
- Unanticipated Problem / Adverse Event Report Form
Emergency Use
- Emergency Drug Treatment Form
- Expanded Access Medical Device Form
- Physician Checklists for Emergency/Off Label Use
Consent Templates
- Biomedical Research Consent updated 4/27/2012
- Social/Behavioral Research Consent updated 4/27/2012
- Specimens/Data Repository Consent
- Specimens/Data Repository Language to Insert in Biomedical Consent
- Sample Assent Form for Children
- Research Subject Information Sheet Template
- International Research Consent added 5/8/2012
- Short Consent Form - English
- Short Consent Form - Spanish
- Short Consent Form for Children - Spanish
Research Documentation Templates and Checklists
- Consent Documentation Template
- Legally Authorized Representative Documentation Template
- Legally Authorized Representative Investigator Assurance Form
- Research Organizational Checklist (ROC)
