References
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1.9 Resources Necessary to Protect Subjects
Last Revised: 1/16/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s ...
8.2 Review of Study Related Complaints
Last Revised: 5/8/2023 1.0 Purpose The purpose of this policy is to describe the process for repo...
8.7 Reporting Incidents to Institutional Officials and Federal Agencies
Last Revised: 8/1/2023 1.0 Purpose The purpose of this policy is to describe the Organization’s r...
8.1 Review of Adverse Events and Adverse Device Effects
Last Revised: 10/2/2024 1.0 Purpose The purpose of this policy is to describe the process for rep...
8.4 Review of Noncompliance by the PI, Study Team, and/or Subjects
Last Revised: 8/6/2025 1.0 Purpose The purpose of this policy is to describe the process for revi...
Table of Contents
Section 1: General Human Research Protection Program Polices 1.1 Human Research Protection Progra...
2.9 Closure of On-Going Research
Last Revised: 08/10/2023 For an abbreviated version intended for investigators, coordinators, and...
2.7 Continuing Review of Research
Last Revised 1/12/2024 For an abbreviated version intended for investigators, coordinators, and s...
3.2 Data and Safety Monitoring
Last Revised 12/22/2022 For an abbreviated version intended for investigators, coordinators, and ...
2.2 Full IRB Review
Last Revised: 6/12/2024 For an abbreviated version intended for investigators, coordinators, and ...
1.21 Post-Approval Monitoring of Research
Last Revised: 11/17/2025 For an abbreviated version intended for investigators, coordinators, and...