Office of Research Compliance

IRB Forms 

**  Effective immediately, all IRB submissions must include CITI training completion reports for all investigators.  **

To submit a new proposal for review:

IRB Project Outline Form


Consent Form Templates

Adult Consent Form with Signature

Adult Consent Form without Signature

Parental Consent Form

Online Consent Form

 

To submit a change to an approved proposal:

IRB Amendment Form

 

To renew a study:

IRB Periodic Review Form

 

To report an event to the IRB:

For guidance on reporting unanticipated problems involving risks to subjects or others and adverse events, please consult with the Office of Research Compliance, 593-0664, or refer to the guidance from OHRP on this website:

http://www.hhs.gov/ohrp/policy/advevntguid.html

Event Reporting Form