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
You can find the recordings from our recent IRB Brown Bag and Boot Camp presentations on our YouTube channel, or browse the links below.
| Date | Presenter/Title | Resources |
| April 13, 2022 | Protocols, Recruitment, and Consent (presented by Lauren Griffin, PhD) | Slides / Video |
| March 09, 2022 | Study Recruitment and Social Media (presented by Elizabeth Flood-Grady, PhD) | Slides / Video |
| February 09, 2022 | IRB Basics for Student Researchers (presented by Lauren Griffin, PhD) | Slides / Video |
| January 12, 2022 | UF IRB Discretionary Policy Updates & IRB Roundtable Discussion (presented by Peter Iafrate, PharmD, and Ivana Simic, PhD) | Video |
| November 10, 2021 | UF Human Subject Payments (HSP) Services (presented by Brenda Harrell) | Slides / Video |
| September 29, 2021 | Who Can Consent When the Subject Can’t? (presented by Dianne Farb, JD) | Slides / Video |
| November 10, 2021 | Smart Forms: What does the IRB look for? (presented by Lauren Griffin, PhD) | Slides / Video |
| April 28, 2021 | Open Access Data Banks and sIRB Made Simple (presented by Peter Iafrate, PharmD, and Ivana Simic, PhD) | Open Access Data Banks slides / sIRB Made Simple slides / Video |
| February 8, 2021 | IRB Boot Camp: Strong Submissions, Strong Research (presented by Lauren Griffin, PhD) | Slides / Video |
| December 9, 2020 | IRB Blunders to Avoid (presented by Tanya Aranca) | Slides |
| November 18, 2020 | Data/Chart Review Training (presented by Ivana Simic, PhD) | Slides |
| March 11, 2021 | Informed Consent Training (presented by Tanya Aranca) | Slides |
| February 12, 2020 | The Common Rule sIRB Mandate (presented by Ivana Simic, PhD) | Slides |
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