Office of Research Compliance

IRB Forms 

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

To submit a new proposal for review:

IRB Project Outline Form

 

Consent Form Templates

Adult Consent Form

Consent Form with Waiver of Signature

Parental Consent Form

Online Consent Form

For assistance in completing the Project Outline Form

IRB Guidelines

 

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