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 |
Version Date |
|---|---|
| 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 |