Helpful Links

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

IRB Processes

• IRB Process Flowchart

• Submission Process

• Institutional Risk Assessment for Cooperative Groups and Investigator Initiated Studies

• Cancer Related Studies - What's needed PRIOR to IRB submission.
  Effective September 15, 2003, ALL cancer related studies should be reviewed and approved by the OU Cancer Center Scientific Review Committee prior to IRB submission of a New Project Application.

• SRC Policy Regarding Tissue Studies

• Consent Process Discussion

• Expedited Review - Criteria
• Exempt Review - Criteria

• Radiation Safety Review - It is preferred that Radiation Safety review be conducted prior to IRB review.