1. Radiation Committee Review (AURPAC), (See also item #5, "Department of Radiology Review Committee")

2. Institutional Biosafety Committee Review

3. General Clinical Research Center (GCRC)

4. Investigational Drug Services (IDS)

• The IRB review application requests an IDS number. This is the internal number generated by the IDS.
• All clinical trials involving investigational agents must be registered with the IDS regardless of whether or not you are going to use their services. If you do not plan on using the investigational pharmacy to dispense the study medications, please complete this form. To download an application, go to www.fairview.org/prof/research/PDF/forms/form4.PDF
• The application must have the following items included:
  • Form 1572
  • Protocol
  • Investigational Drug Brochure
  • Copy of IRB approval (when available)
  • Copy of the IRB-approved consent form (Note: For the BMT Program, this information is supplied automatically by the BMT Administrative Office.)

5. Department of Radiology Review Committee

All protocols with a radiation therapy component must be submitted to the University's Department of Therapeutic Radiology for review and approval. This approval must be obtained prior to submission to AURPAC. Download an application for departmental review (MSWord doc).