Human Research Protection Program

Biomedical IRB and Biomedical Cancer IRB Submissions

PLEASE NOTE:  Beginning October 29th, To submit NEW PROTOCOLS, IRB Manager Software will replace KUALI COEUS (KC). 

KUALI COEUS (KC) Will only be used for Approved data/studies that already exist in the KC system.

 For more information: IRB MANAGER INFORMATION PAGE

If you have an ONGOING, LONG-TERM STUDY with an IRB# that begins in the 100 series, please continue to submit the AMENDMENT, CONTINUING REVIEW, DEVIATION and FINAL REPORT documents listed below.

Thank you for your patience as we transition to the new electronic system!
 

BIOMEDICAL/CANCER IRB FORMS

Adverse Events

 
 
 
 
 
 
Continuing Review
Amendments/Modifications Waiver of Authorization
Miscellaneous Forms Final Reports
Consent Forms Compliance Forms

  Central IRB Submission Information
 
The first two documents apply to the initial submission process for both WIRB
& Advarra. The third document is to be used to notify the UT HRPP of Personnel Changes to a CIRB reviewed study.

 
 
Last Updated: 6/30/19