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1. irb.ufl.edu › irb01 › formsTemplate & IRB Forms » Institutional Review Board - University of...

   irb.ufl.edu › irb01 › forms

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   IRB Forms, Templates & Tools. Alphabetical List of IRB-01 Forms; Informed Consent Forms; Obtaining Consent: Special Considerations; Standardized Text for Informed Consent Forms; Glossary of Lay Terms for Use in Informed Consent Forms; Study Related Checklists; Documentation Tools; Education. Education Home; UF IRB Educational Courses ...

   • Alphabetical Listing of IRB-01 Forms - University of Florida

     Continuing Review for sIRB Studies Only (UF IRB of record)...

   • Institutional Review Board » University of Florida

     New: If you intend to submit a non-human or exempt study,...

2. irb.ufl.eduInstitutional Review Board » University of Florida

   irb.ufl.edu

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   New: If you intend to submit a non-human or exempt study, you might be eligible for an instant auto-determination without submitting a study to the IRB. To get an instant determination, please use the non-human/exempt auto-determination tool.

3. guides.uflib.ufl.edu › Clinical_Research › IRBIRB - Clinical Research - Guides @ UF at University of Florida

   guides.uflib.ufl.edu › Clinical_Research › IRB

   29 Οκτ 2024 · Researcher Manual (pdf) step-by-step instructions for using myIRB. IRB Submission Information. Review IRB forms information: IRB Forms. Alphabetical list of IRB01 forms. Form for instruments that do not need to be submitted to the IRB as they have already been assessed.

4. my.irb.ufl.eduFolder Navigator - University of Florida

   my.irb.ufl.edu

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   If you intend to submit a non-human or exempt study, you might be eligible for an instant auto-determination without submitting a study to the IRB. To get an instant determination, please use the non-human/exempt auto-determination tool.

5. med.jax.ufl.edu › research › institutional-review-board-resourcesInstitutional Review Board Resources | College of Medicine ...

   med.jax.ufl.edu › research › institutional-review-board-resources

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   Self Registration Service for Exempt, Non-Human Subjects, and QI Projects. The IRB has a self-registration service for certain exempt, non-human subjects, and QI projects. Visit the UF Division of Research Operations and Services to see if your research qualifies for self-registration.

6. facultyaffairs.med.ufl.edu › wordpress › filesElements of the IRB Process - University of Florida

   facultyaffairs.med.ufl.edu › wordpress › files

   • Per the university policy, UF IRBs make exempt determinations, not the PI (non-human and exempt based on a category) o The policy is grounded in OHRP guidance on non-human research involving coded and de-identified tissue and pragmatic considerations regarding expertise required to assign exempt categories. 20

7. research.ufl.edu › uploads › 7IRB BASICS AND CONSENT CONSIDERATIONS - UF Research

   research.ufl.edu › uploads › 7

   Define “IRB”. Give a brief history of human subjects’ research. Define IRB terminology. Give helpful resources for research. Review Researcher Responsibilities. Review informed consent as a “process”. Review requirements of human subjects’ research. Federal policy. UF policy.