IRB Policies & Procedures
10.3 Research Integrity / Institutional Review Board
- 10.3.1 Human Research Protection Program- Governing Principles, Policy and Organizational Structure
- 10.3.2 Research Subjects with Cognitive Impairment
- 10.3.3 Defining Human Subjects Research
- 10.3.4 International Research
- 10.3.5 Serious Adverse Event and Unanticipated Problems Reporting
- 10.3.6 Children in Research
- 10.3.7 Disclosure and Use of PHI in Research
- 10.3.8 University Students as Research Subjects
- 10.3.9 Closing an IRB Approved Study
- 10.3.10 Informed Consent
- 10.3.11 Waiver of Informed Consent
- 10.3.12 Use of Drugs and Biologics in Human Subjects Research
- 10.3.13 Use of Devices in Human Subject Research
- 10.3.14 Continuing Review of IRB Approved Studies
- 10.3.15 Protocol Deviations
- 10.3.16 Research Registries and Repositories
- 10.3.18 Institutional Authorization Agreements (IAA) and Reliance Agreements