Other Resources
The University of Florida will be developing more training materials for Investigators in the future. This page only represents a beginning. We hope to develop training materials that are specific to all areas of research conducted at UF. Please forward your training and education suggestions to the IRB Office.
Educational Event Recordings
Brown Bags:
- February 12, 2025 – Introduction to the UF CTSI Services
Link to February Zoom Recording – Pending Session
- January 15, 2025 – Continuing Reviews & Status Reports
Link to January Zoom Recording – Pending Session
- December 11, 2024 – IRB Submission Best Practices and Q&A
Link to December Zoom Recording
- November 11, 2024 – How to Build a Strong ICF
Link to November Zoom Recording
- October 16, 2024 – ClinicalTrials.gov – Part 2
Link to October Zoom Recording
- September 11, 2024 – IRB Fall Boot Camp: Intro to myIRB and Submission Basics
Link to September Zoom Recording
- August 14, 2024- Intro to HURRC
https://mediasite.video.ufl.edu/Mediasite/Play/5b0dbfce8c3a49b898bb16e93f902b131d
- July 10, 2024-Ceding Review to an External IRB
https://mediasite.video.ufl.edu/Mediasite/Play/92ce5095507548fb9ed568826dd972561d
- June 12, 2024- How to Submit a Strong Revision
https://mediasite.video.ufl.edu/Mediasite/Play/eeffba46c2f5477d9dc3f6b03aec15e21d
- May 22, 2024- Recruiting & Advertising for Research Participants
https://mediasite.video.ufl.edu/Mediasite/Play/d85322d951d44cf4adb00e831cb122551d
- April 10, 2024 – ClinicalTrials.gov – Part 1
https://mediasite.video.ufl.edu/Mediasite/Play/88600dda29904f919d3e816e11cbbe9f1d
- March 13, 2024- Auto determination Tools
https://mediasite.video.ufl.edu/Mediasite/Play/fe5ceb4869c647808cfc828fb412cb4e1d
- February 28, 2024- REDCap for eConsent
https://mediasite.video.ufl.edu/Mediasite/Play/4358c4a9444d4ff6a8a1006e5bfdf3ab1d
- January 17, 2024 – New Guidelines: Pregnancy Testing in Research & Minor Increase in Minimal Risk
https://mediasite.video.ufl.edu/Mediasite/Play/3d58040d486b4285ae606cf6d4b861bf1d
Other Useful Federal Web Sites
- Center for Disease Control and Prevention (CDC)
- Code of Federal Regulations
- Federal Regulations for Human Subject Research (45 CFR 46)
- FDA (Food and Drug Administration)
- FDA (Food and Drug Administration) IRB Information Sheets
- Frequently Asked Questions on Botanical Drug Product Development – FDA guide to studying food additives.
- International Conference on Harmonization (ICH)
- National Bioethics Advisory Commission
- National Institutes of Health (NIH)
- NIH Grants & Funding Opportunities
- NIH Bioethics Resources
- National Science Foundation (NSF)
- Office of Justice Programs (OJP)
- OHRP (Office for Human Research Protections) (formerly OPRR)
- OHRP IRB Guidebook Human Subject Protections
- OHRP- Human Subject Regulations Decision Charts
- OHRP Determination Letters
- U.S. Department of Education (DOE)
- U.S. Department of Health and Human Services (DHHS)
Other Links
- Jesse’s Intent Presentation by Paul Gelsinger, October 31, 2000, San Diego , CA