Alphabetical Listing of IRB-01 Forms
Title | Revision | |
---|---|---|
Addenda | ||
A: Researcher Assurance | ||
Assurance letter for NIH Certificate of Confidentiality | 03/03/2020 | |
Closure Certification for Biologic Specimens Bank | 03/11/2016 | |
Confidentiality Agreement for Data and/or Specimens | 03/11/2016 | |
Continuing Review for sIRB Studies Only (UF IRB of record) | ||
Adverse Event Summary Table (sIRB only) | 01/07/2020 | |
Deviation Tracking Log (sIRB only) | 01/07/2020 | |
Subject Enrollment (sIRB only) | 01/07/2020 | |
Cumulative Adverse Event Table for Continuing Review | 03/17/2017 | |
EXCEL version | ||
Cumulative Deviation Table for Continuing Review | 05/09/2013 | |
Data Sharing Form Template | 11/08/2019 | |
Emergency Use | 10/07/2019 | |
Emergency Use Checklist | 11/02/2016 | |
Emergency Use Consent (if one not available from sponsor) | 12/15/2006 | |
Emergency Use Independent Physician Certification | 06/13/2008 | |
Adverse Event Reporting Form | ||
GWAS Data Sharing Plan Template | 06/07/2017 | |
HIPAA – Certificate for Preparatory Research (UF/Shands version) | 03/11/2016 | |
HIPAA – Certificate for Research with Decedents Info (UF/Shands version) | 03/11/2016 | |
HIPAA – Disclosure Tracking Log: Research | Live | |
HIPAA – Stand-alone Authorization Form | 03/15/2019 | |
Informed Consent Forms | Live | |
Use this link to visit a separate page dedicated to Informed Consent Forms. All of the different templates are available as well as other resources and instructions. | ||
Introductory Questionnaire for Data Transfer Studies | 03/11/2016 | |
This is only to be used by faculty who are new to / joining UF who are simply bringing their previously collected research data with them for continued analysis. No additional study interventions or data collection remain. A: Researcher Assurance | ||
Principal Investigator Change | 06/13/2008 | |
Revision to permanently change the PI – signed by the old/departing PI and the new PI must also submit a revision in myIRB. Note: changing the PI on a study that is normally reviewed at the full Board must also be reviewed at full Board, so please take note of our full Board deadlines /irb01/deadlines.html. | ||
Protocol | 03/09/2004 | |
Sample protocol with helpful information to remember/consider when writing your protocol. Read Protocol Template Guidelines before completing the protocol form. You may use the sponsor’s protocol or GCRC protocol if available. | ||
Quality Improvement vs Research Determination Form | 10/25/2019 | |
Unaffiliated Investigator Agreement (OHRP’s Individual Investigator Agreement) | 05/23/2017 | |
Visiting Researcher Agreement | 08/20/2019 |