| Research Credentialing | 07/07/2022 | 07/07/2027 |
| Research Records Management | 07/07/2022 | 07/07/2027 |
| Research and Development Committee (RDC) Operating Procedures | 02/11/2022 | 02/28/2027 |
| Request for Research vs. Non-Research Operations Evaluation | 08/02/2018 | |
| RDC Project Status Update and Continuing Review | 04/01/2021 | 04/30/2026 |
| Human Research Protection Program (HRPP) Standard Operating Procedures | 04/07/2022 | 04/07/2027 |
| National Cancer Institute's Central IRB | 01/05/2023 | 01/05/2028 |
| Documentation in CPRS | 07/11/2023 | 07/11/2028 |
| CPRS Medical Records for Non-Veteran Research Subjects and Veterans Not Currently Enrolled in the VA System | 06/01/2023 | 05/31/2028 |
| Flagging Medical Charts of Patients Involved in Medical Research Studies | 04/07/2022 | 04/06/2025 |
| Collection and Storage of Regulatory Documents | 01/05/2023 | 01/05/2028 |
| Research Clinics | 06/01/2023 | 06/01/2028 |
| Study Monitoring Visits-Process for Access to Information and Reporting of Site Visit Results | 11/17/2022 | 11/17/2027 |
| VA Research Study Monitor Report | 11/17/2022 | |
| Use of the VA Central IRB | 04/13/2023 | 04/12/2028 |
| Submission of Informed Consent Documents and other Signed Authorizations | 02/03/2022 | 02/03/2025 |
| Research Personnel Notification of Pharmacy Benefits Management Drug Safety Alerts and Adverse Drug Events | 06/01/2017 | 05/31/2020 |
| Sponsor Adverse Event/Unanticipated Problems Reporting - Device | 06/02/2022 | 06/02/2025 |
| Sponsor Protocol Deviation Reporting - Device | 06/02/2022 | 06/02/2025 |
| Sponsor Study File Management - Device | 06/02/2022 | 06/02/2025 |
| Sponsor - Unanticipated Adverse Device Effect Reporting (UADE) | 06/02/2022 | 06/02/2025 |
| Use of Western IRB (WIRB) - Copernicus Group (WCG) | 06/04/2020 | 06/03/2023 |
| Use of ADVARRA, Inc. IRB | 06/04/2020 | 06/03/2023 |
| Mayo Clinic Convalescent Plasma | 06/04/2020 | 06/03/2023 |
