References
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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...
8.3 Review of Unanticipated Problems Involving Risk to the Subject or Others
Last Revised: 8/6/2025 1.0 Purpose The purpose of this policy is to describe the process for repo...
2.4 IRB Review of Changes in Previously Approved Research
Last Revised 1/18/2025 For an abbreviated version intended for investigators, coordinators, and s...
2.7 Continuing Review of Research
Last Revised 1/12/2024 For an abbreviated version intended for investigators, coordinators, and s...
2.3 Expedited Review
Last Revised 1/24/2024 For an abbreviated version intended for investigators, coordinators, and s...
2.2 Full IRB Review
Last Revised: 6/12/2024 For an abbreviated version intended for investigators, coordinators, and ...
1.26 PI Qualifications and Responsibilities
Last Revised: 6/11/2025 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...
1.29 ClinicalTrials.gov Reporting
Last Revised: 3/9/2026 1.0. Purpose The purpose of this policy is to describe the requirements fo...
1.33 Posting of Clinical Trial Consent Forms
Last Revised: 3/16/2026 1.0 Purpose The purpose of this policy is to describe the Organization’s ...
5.1 Obtaining Informed Consent From Research Subjects
Last Revised: 5/13/2026 For an abbreviated version intended for investigators, coordinators, and ...