Guidance documents are supportive documents that either describe in detail how a specific procedure is required to be performed or suggest direction on operational processes and workflows. These guidance documents have been developed by University offices with relevant knowledge and/or expertise. Some documents identify mandatory processes; however, all documents are being shared as resources.
*Please check with your group regarding supplemental guidelines established by your department.
Guidance Document Title
|Clinical Trial Agreement (CTA) Guidance||April 2022|
|MTA/DTA Processes for Review and Signature Approval By University of Utah Human Research Protection Program (HRPP) Units||April 2022|
|Non-Industry Fee Schedule / Site Budget Guidance||November 2022|