OUHSC HRPP / IRB 

Forms & Templates

Consent Forms

Research Privacy Forms (HIPAA)

 HIPAA Webpage
 

Other Study Documents

 

  • Protocol Outline
     

  • Modification Summary Report
          For use in tracking Modifications that are submitted to the IRB (and approved); to be reported at the time of Continuing Review.
     

  • Protocol Deviation Summary Report
          For use in tracking all deviations - major and minor - to be reported at the time of Continuing Review. (See HRPP SOP 407 for more information and guidance regarding deviations) 
     

  • Summary of Participant Harms Report
          For use in tracking all harms - anticipated and unanticipated; outside and local - to be reported to the IRB at the time of Continuing Review.

 

Spanish/Translated Documents

Study-Related Submission Forms

Other IRB Submission Forms (not study-related)