Follow Research Workflows
Review the Manage Study section of our website to learn about all of the research workflows that may apply to your study during the different timepoints of the study’s lifecycle.
Before Starting a Study
Prior to starting your study in a UF Health location, you may be required to submit your study to various review committees to ensure that your study details are communicated to Shands staff and that research workflows are followed. See Human Subjects Research Reviews for more details.
Procedure Coding Requests (PCR)
If study team will be obtaining the procedure codes, study team requests using the following form(s):
- Operating Room – Technical PCR Form – Version 02/02/10
- Operating Room – Surgery Professional PCR (use generic form)– Version 06/30/17
- Operating Room – Anesthesiology Professional PCR (use generic form) – Version 06/30/17
Investigational Devices Used in OR
Study teams must use the Device Trial Listserv prior to using or implanting a device being investigated in an Investigational Device Exemption (IDE), Carotid Artery Stent(CAS) , or Coverage with Evidence Development (CED) study. See Device Trial Listserv for more information.