Document Name
| Document Type | Previous Version | Previous Date | New Version | New Date |
| IRB Policy 1.10 Suspension or Termination of IRB Approval | Policy | 4.02 | 6/19/2017 | 5.00 | 1/21/2019 |
| IRB Policy 1.11 Reporting Obligations for Principal Investigators | Policy | 5.02 | 7/3/2017 | 5.03 | 1/21/2019 |
| IRB Policy 1.14 Determining when Activities are Research or Research Involving Human Research Participants | Policy | 2.06 | 6/15/2015 | 3.00 | 1/21/2019 |
| IRB Policy 1.2 Federalwide Assurance | Policy | 6.00 | 7/3/2017 | 7.00 | 1/21/2019 |
| IRB Policy 1.3 Committee Structure | Policy | 6.07 | 11/28/2015 | 7.00 | 1/21/2019 |
| IRB Policy 1.5 Member Conflict of Interest | Policy | 5.03 | 7/3/2017 | 5.04 | 1/21/2019 |
| IRB Policy 1.6 Meeting and Meeting Records | Policy | 9.04 | 7/3/2017 | 10.00 | 1/21/2019 |
| IRB Policy 1.7 Risks To Research Participants | Policy | 2.05 | 7/3/2017 | 2.06 | 1/21/2019 |
| IRB Policy 1.8 Approval Date Guidelines and Turnaround Times | Policy | 8.01 | 7/3/2017 | 9.00 | 1/21/2019 |
| IRB Policy 1.9 Noncompliance | Policy | 4.05 | 6/19/2017 | 5.00 | 1/21/2019 |
| IRB Policy 2.1 New Application | Policy | 8.00 | 11/20/2017 | 9.00 | 1/21/2019 |
| IRB Policy 2.4 Emergency Use of an Investigational Drug or Device | Policy | 6.02 | 6/15/2015 | 7.00 | 1/21/2019 |
| IRB Policy 2.5 Modification to On-Going Activities | Policy | 7.00 | 11/20/2017 | 8.00 | 1/21/2019 |
| IRB Policy 2.6 Unanticipated Problems Involving Risks to Subjects or Others | Policy | 6.05 | 6/19/2017 | 7.00 | 1/21/2019 |
| IRB Policy 2.8 Requirements for Reporting to Institutional and External Officials | Policy | 9.00 | 4/2/2018 | 10.00 | 1/21/2019 |
| IRB Policy 2.9 Closure and Re-Open | Policy | 4.00 | 7/3/2017 | 5.00 | 1/21/2019 |
| IRB Policy 2.10 Research Participant Inquiries | Policy | 3.04 | 7/3/2017 | 3.05 | 1/21/2019 |
| IRB Policy 2.12 Privacy and Confidentiality | Policy | 3.04 | 7/3/2017 | 4.00 | 1/21/2019 |
| IRB Policy 2.13 Use of Interpreter Services and Translated Documents | Policy | 5.05 | 5/14/2013 | 6.00 | 1/21/2019 |
| IRB Policy 2.14 Multi-Center Study Coordination - IRB Review and Oversight | Policy | 8.00 | 7/3/2017 | 9.00 | 1/21/2019 |
| IRB Policy 2.15 Research Involving Special Populations | Policy | 6.01 | 7/3/2017 | 7.00 | 1/21/2019 |
| IRB Policy 2.16 Monitoring of Institutional Review Board, IRB Operations, and Research Studies | Policy | 8.00 | 9/4/2018 | 9.00 | 1/21/2019 |
| IRB Policy 2.17 Maintenance and Retention of IRB Documents | Policy | 3.03 | 7/3/2017 | 4.00 | 1/21/2019 |
| IRB Policy 2.18 Funding Source Document (FSD) Review | Policy | 9.00 | 11/20/2017 | 10.00 | 1/21/2019 |
| IRB Policy 2.2 Continuing Review | Policy | 8.00 | 11/20/2017 | 9.00 | 1/21/2019 |
| IRB Policy 2.24 IRB Reliance Agreements | Policy | 3.00 | 7/3/2017 | 3.01 | 1/21/2019 |
| IRB Policy 2.25 Identification and Use of Legally Authorized Representatives | Policy | 1.01 | 12/7/2009 | 2.00 | 1/21/2019 |
| IRB Policy 2.26 Research Involving Department of Defense Components / DoD | Policy | 3.01 | 7/3/2017 | 4.00 | 1/21/2019 |
| IRB Policy 2.28 Status Reports for IRB Files | Policy | - | - | 1.00 | 1/21/2019 |
| IRB Form Adverse Event Reporting | Form | 4.03 | 8/1/2016 | 5.00 | 1/21/2019 |
| IRB Form Application for Review Human Specimens or Data Research | Form | 7.00 | 1/21/2019 | 7.01 | 1/21/2019 |
| IRB Form Application for Review Interventional Research | Form | 7.00 | 1/21/2019 | 7.01 | 1/21/2019 |
| IRB Form Application for Review Observational Research | Form | 8.00 | 1/21/2019 | 8.01 | 1/21/2019 |
| IRB Form Consent Form Template: Clinical Research | Consent Form Template | 12.00 | 12/22/2017 | 13.00 | 1/21/2019 |
| IRB Form Consent Form Template: Minimal Risk | Consent Form Template | 7.00 | 12/22/2017 | 8.00 | 1/21/2019 |
| IRB Form Consent Form Template: Minimal Risk Studies | Consent Form Template | 7.00 | 12/22/2017 | 8.00 | 1/21/2019 |
| IRB Form Consent Form Template: Public Health Sciences (PHS) | Consent Form Template | 5.00 | 12/22/2017 | 6.00 | 1/21/2019 |
| IRB Form Consent Form Template: Public Health Sciences (PHS) Minimal Risk Research | Consent Form Template | 5.00 | 12/22/2017 | 6.00 | 1/21/2019 |
| IRB Form Continuing Review Report | Form | 7.00 | 7/3/2017 | 8.00 | 1/21/2019 |
| IRB Form Expedited Reporting Form for Unanticipated Problems or Noncompliance | Form | 3.00 | 8/1/2016 | 4.00 | 1/21/2019 |
| IRB Form Expedited Review Checklist for Minimal Risk Activities | Form | 2.02 | 8/1/2016 | 2.03 | 1/21/2019 |
| IRB Form External IRB Cover Sheet - New Application | Form | 4.00 | 5/29/2018 | 5.00 | 1/21/2019 |
| IRB Form Funding Source Supplement | Form | 7.01 | 7/3/2017 | 8.00 | 1/21/2019 |
| IRB Form Glossary of Terms and Acronyms | Form | 6.00 | 3/19/2018 | 7.00 | 1/21/2019 |
| IRB Form Human Subjects Research Determination Form | Form | 5.00 | 6/4/2018 | 5.01 | 1/21/2019 |
| IRB Form Individual Investigator Agreement | Form | 2.01 | 7/3/2017 | 2.02 | 1/21/2019 |
| IRB Form Interpretation Certificate | Form | 1.01 | 8/1/2016 | 2.00 | 1/21/2019 |
| IRB Form Multi-Center Supplement | Form | 6.00 | 7/3/2017 | 7.00 | 1/21/2019 |
| IRB Form Pre-Reviewed Sources of De-Identified Human Specimens and/or Data | Form | 1.08 | 6/8/2017 | 1.09 | 1/21/2019 |
| IRB Form Repository, Registry, or Databank Supplement | Form | 2.03 | 8/1/2016 | 3.00 | 1/21/2019 |
| IRB Form Research Modification | Form | 7.00 | 11/20/2017 | 8.00 | 1/21/2019 |
| IRB Form Third-Party Safety Report | Form | 5.00 | 8/1/2016 | 6.00 | 1/21/2019 |