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IRB Policies & Procedures
10.3 Research Integrity / Institutional Review Board
- 10.3.1 Human Research Protections Program- Governing Principles, Policy and Organizational Structure
- 10.3.2 Human Subjects Research (HSR) Determinations
- 10.3.3 Human Subjects Research Protection Training
- 10.3.4 International Research
- 10.3.5 Reporting Serious Adverse Events and Unanticipated Problems
- 10.3.6 Research with Vulnerable Populations
- 10.3.7 Disclosure and Use of Protected Health Information (PHI) in Research
- 10.3.8 Students as Research Subjects
- 10.3.9 Closing an IRB Approved Study
- 10.3.12 FDA Regulated Products in Human Subject 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