Unless otherwise specified, all forms should be delivered to Armour Academic Center, Room 544. For more information, call (312) 942-5498.

• Coverage Analysis Routing Form (PDF, 75k)
  A Coverage Analysis Must Be Done Before IRB Submission.

• Coverage Analysis (PDF, 66k)
  - Steps before submission of a Clinical Trial to the IRB.

• New Project Form (PDF, 227k)
  This form replaces all of the following: 8-page application for new projects, expedited review form, and the exemption form.

• Consent Document (PDF, 129k)
  As of 11/24/04, the consent template has changed! Please review/incorporate the new suggested language.

• Amendment Form (PDF, 103k)
  This form must be submitted along with any request for changes to a protocol.

• Continuing/Annual Review Reporting Form (PDF, 457k)
  This form replaces the Progress Report and must be accompanied with any request for renewal of approval.

• Serious, Unexpected or Unanticipated Adverse Event Reporting Form (PDF, 112k)
  This form must be submitted when reporting a serious, unexpected or unanticipated event. Please be sure to include one copy of the currently stamped, approved consent document with this report.

• Termination Form (PDF, 57k)
  This form must be submitted when reporting that a study has been permanently and finally closed at the Medical Center.

• Informed Consent Repository form (PDF, 73k)

• Guide for Ads (PDF, 80k)

• Data/Tissue Repository Application (PDF, 57k)

• Regarding the Emergency Use of an unapproved medical device or drug

• Modifications to WIRB® Submission and SAE Forms
  Last updated 3/1/00. This material is ONLY for those investigators who the Rush IRB permitted to access WIRB® (prior to June 1999). Rush investigators must now use the Rush IRB.

• Investigational Drug Data Sheet (PDF, 204k)

• Investigational Device Data Sheet (PDF, 49k)

• Research Specific HIPAA Forms