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IRB Submission Process


The application form, protocol, consent form (if necessary), and supporting documents for all New Studies should be submitted using the iRIS - Integrated Research Information System.  Log into iRIS at: https://iris.ouhsc.edu

The IRB Application should include the following:

  • CONSENT FORM(S)  (See Consent Form Template on Forms page)
  • INVESTIGATOR'S BROCHURE  (Required if study includes experimental drug or device.)
  • QUESTIONNAIRES/SURVEYS  (Required, if used.)
  • ADVERTISEMENTS  (Radio, TV, Newspaper, Posters, Handouts, Press Releases, Interviews if information pertains to a specific study)
  • HIPAA - Include appropriate Research Privacy Form(s).


SRC Review Prior to IRB Submission:
Effective 09/15/03 all cancer related protocols are required to be submitted to the Scientific Review Committee (SRC) at the Peggy and Charles Stephenson Cancer Center at The University of Oklahoma (OU Cancer Center) prior to IRB submission. Visit the OU Cancer Center website for required SRC forms and information about the role and procedures of the SRC.



Institutional Review Board (IRB) - OU Health Sciences Center
Library Building, Room 176
Phone: 405/271-2045 - Fax: 405/271-1677

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