Alphabetical Listing of IRB-01 Forms
| Title | Revision | |
|---|---|---|
| Addenda | ||
| We now only accept new studies within myIRB. Most of these Addenda have been built into the myIRB system and are here only for those studies that have already been approved in a paper version and may require a Project Revision.
F: Radiation or Radioactive Materials G: Gene Therapy or Genetic Testing |
||
| Adverse Event Reporting Form | 03/11/2016 | |
| Reporting Guide Definitions | ||
| Closure Report: no subjects enrolled | 03/11/2016 | |
| Closure Report: subjects enrolled | 03/11/2016 | |
| Closure Report: tissue/data banks | 03/11/2016 | |
| Closure Certification for Biologic Specimens Bank | 03/11/2016 | |
| Confidentiality Agreement for Data and/or Specimens | 03/11/2016 | |
| Continuing Review | 03/11/2016 | |
| Continuing Review Requirements (updated 4/16/2007) When should you submit your Continuing Review Report? | ||
| Continuing Review for TISSUE/DATA banks | 03/11/2016 | |
| Continuing Review Requirements (updated 4/16/2007) When should you submit your Continuing Review Report? | ||
| CQI vs. Research Protocol Form | 01/30/2014 | |
| Cumulative Adverse Event Table for Continuing Review | 03/17/2017 | |
| EXCEL version | ||
| Cumulative Deviation Table for Continuing Review | 05/09/2013 | |
| Deviation/Non-Compliance Reporting Form (single occurence, reporting in 5 days) | 03/11/2016 | |
| Reporting Guide & Definitions | ||
| Emergency Use | 03/11/2016 | |
| 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 | |
| Explicit Change Response | 03/11/2016 | |
| Full Board Meeting Correction | 12/08/2016 | |
| GWAS Data Sharing Plan Template | 06/07/2017 | |
| HDE – new submission | 03/11/2016 | |
| HDE Continuing Review/Closure | 03/11/2016 | |
| Humanitarian Use Device with Humanitarian Device Exemption | ||
| 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 | |
| For research that has obtained a Waiver of HIPAA Authorization. Link will take you to the Privacy Website. | ||
| HIPAA – Waiver of Authorization | 03/11/2016 | |
| What’s different since the last version? | ||
| 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 | ||
| Introductory Questionnaire for Full Board and Expedited Studies | 02/24/2012 | |
| We no longer accept any new studies on any paper versions of the IQ form listed above. New protocols of these types must be submitted via myIRB. | ||
| Introductory Questionnaire for Nonhuman/Exempt Studies | 07/06/2012 | |
| We no longer accept any new studies on any paper versions of the IQ forms above. New protocols of these types must be submitted via myIRB. | ||
| Introductory Questionnaire for Retrospective Record/Chart/Data Review Studies | 07/05/2012 | |
| We no longer accept any new studies on any paper versions of the IQ forms above. New protocols of these types must be submitted via myIRB. | ||
| Introductory Questionnaire for Tissue/Data Banks | 02/28/2013 | |
| We no longer accept any new studies on any paper versions of the IQ forms above. New protocols of these types must be submitted via myIRB. | ||
| 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 the Revision form. 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. | ||
| Principal Investigator Proxy Request | 03/11/2016 | |
| For Paper Studies: Individuals added as a Proxy Co-PI must: 1) Be listed on your Addendum A 2) Be qualified to oversee the protocol in a similar manner to the PI For myIRB studies: There is an option to add an Investigator as a PI Proxy. | ||
| 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. | ||
| Psychological and Survey Measure Form | 11/12/2010 | |
| For new research that expects to use these types of measures with human participants. | ||
| Revision | 03/11/2016 | |
| Tabled Submission Response | 12/08/2016 | |
| Title Verification Form (DSR Form) | 05/10/2013 | |
| Temporary Transfer of Study Responsibility | 03/11/2016 | |
| Unaffiliated Investigator Agreement (OHRP’s Individual Investigator Agreement) | 05/23/2017 | |
| Unanticipated Problem Reporting Form | 03/11/2016 | |
| Reporting guide Definitions |
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