Clinical Sites

Click on the excel icon to view a list of University Health System Clinical Sites.   Arrows at the top of the columns allow you to filter by clinical site or department.

NON-Research

Activities are not research if they do not involve a systematic approach involving a predetermined method for studying a specific topic, answering a specific question, testing a specific hypothesis, or developing theory.

• UTHSCSA IRB Determination Letter of Non-Research
  
• De-Identified Data Form from UTHSCSA (if applicable)

Research Not Involving Humans

"Research Not Involving Humans" research is conducted with the use of animal specimens, cadaver, left-over, de-identified specimens, or specimens/data from a repository (de-identified to recipient). These studies cross boundaries between basic science and clinical application.
Submit the following:

• Copy of UTHSCSA IRB or  IACUC Approval of Non-human Research Forms
• UHS Research form: Not Involving Humans
• De-Identified Data Plan

Human Use/Exempt

Human use research classified as minimal risk by the Institutional Review Board. 
Submit the following:

• Copy of forms given to UTHSCSA IRB and IRB Approval Letter
• Combined VA/UHS/UTHSCSA Research Scope of Practice
• Copy of IRB dated consent forms (if applicable)
• UHS Institutional Assurance/Supplemental Conditions
  • Document
  • Supplemental Conditions
• UHS Research Protocol Proposal Exempt Form
• Disclosure Log (If Applicable) 

Human Use/Expedited or Full Board

Human use research classified as greater than minimal risk by the Institutional Review Board.
Submit the following:

• Copy of forms given to UTHSCSA IRB and IRB Approval Letter
• Copy of IRB stamped consent form
• Combined VA/UHS/UTHSCSA Research Scope of Practice
• UHS Institutional Assurance/Supplemental Conditions
  • Document
  • Supplemental Conditions
• UHS Research Protocol Proposal Form
• Investigational Device Information Form (Applicable)
• Investigational Drug Information Form (If Applicable)

Humanitarian Device

Submit the following:

• IRB Approval Memo
• FDA Letter Designation of Humanitarian Device
• UHS Form
  • Product Evaluation Approval (Only if UHS required to pay for device)
  • Tracking Plan for Device

Emergency Use

• UHS Policy Information: 9.03000 EMERGENCY USE OF EXPERIMENTAL DRUGS OR DEVICES

Pre-Research

• UHS Forms
• Disclosure Log