Helpful Links

• Food and Drug Administration FDA
  
• Office for Human Research Protections OHRP

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:

• NEW RESEARCH PROJECT APPLICATION FORM

• PROTOCOL
• 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 OU Cancer Center's Scientific Review Committee (SRC) prior to IRB submission. Visit the OU Cancer Center website for required SRC forms and information about the role and procedures of the SRC.