Are you involved with human subject or animal research? The Regulatory and Compliance Office at the College of Pharmacy can help you navigate the numerous institutional, state and federal requirements for conducting research at the University of Florida. We provide assistance with approvals and agreements to ensure your research complies with all applicable regulations and policies.
- Institutional Review Board (IRB) and Institutional Animal Care and Use Committee (IACUC)
Our office can help you plan, prepare and submit documents related to study review, continuing review and study closure.
- Research Administration and Compliance (RAC)
Our office can help obtain confirmation of services and complete billing grids and study registration and initiation checklists.
- ClinicalTrials.gov registration and compliance
Our office can help you obtain your NCT number and maintain your study record on clinicaltrials.gov.
- Data Use, Data Transfer, and Material Use agreements
Let us help you coordinate and submit requests to the Office of Technology Licensing and Privacy Office.
- Academic Honors Submission Review
Our office reviews student requests for academic honors and publications to ensure the research is compliant and following IRB guidelines.
- Sponsor Data Sharing and Publication Requirements
We can assist with the submission of data and publications to public databases.
If you are planning to do research as part of your PharmD program (including for a research elective, honors or within a summer research program such as ISRP or SURF), please complete the following form:
If you are requesting Epic Access, there are two options:
1) Student Access for students who are not employees of UF: http://privacy.ufl.edu/uf-health-privacy/access-to-epic/
Students must complete the following forms and have a mentor’s signature:
2) Research Access for anyone engaged in research and employed by UF.
UF employees must complete the following form and have a either faculty signature or RCO signature:
Completed forms should be sent to this office. RCO will submit the forms to the appropriate administrative offices.
Requirements for participating in a research study:
Find out what training you need to complete by using the Research Training Utility: http://research.ufl.edu/rtu.html
If you are planning to do a Quality Improvement Project, please register with the Quality Improvement Performance Registry:
In order to submit a protocol for review to the IRB you must complete the following steps:
1) Register with myIRB (our electronic IRB submission portal):
2) Complete the required IRB training:
3) For assistance with your IRB submissions be sure to add Ben Burkley to your study team in myIRB:
Trainings and Seminars:
Registration with myIRB and Regulatory and Compliance Q & A
IRB-01 Home Page:
Research Administration and Compliance:
Scholarly Publishing and Academic Resources Coalition (SPARC) data sharing requirements for U.S. funding agencies:
Notice of Proposed Rule Making Summary Document:
For more information about the Notice of Proposed Rule Making (NPRM) to the Common Rule, click this button:
Ben Burkley, MS
Regulatory Research Manager
HPNP Room 3309