Office of Research Compliance

IRB Forms 

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

To submit a new proposal for review:

*NEW FORM* IRB Project Outline Form

 

Consent Form Templates

*NEW FORM* Adult Consent Form with Signature

*NEW FORM*
 Adult Consent Form without Signature

*NEW FORM* Parental Consent Form

*NEW FORM*
 Online Consent Form

 

To submit a change to an approved proposal:

*NEW FORM* IRB Amendment Form

 

To renew a study:

*NEW FORM* 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



*NEW FORM* Event Reporting Form