Standard Operating Procedures
- SOP 101 Training Requirements
- SOP 102 IRB Operations
- SOP 103 Activities Subject to Human Protections
- SOP 104 Scope and Authority of the IRB
- SOP 105 Collaborative Research and Reliance Agreements
- SOP 106 Human Participant Incentive Payment
- SOP 107 Advertising, Recruiting, and Enrolling for Human Subject Research
- SOP 108 Appeal of IRB Decisions
- SOP 109 Change and Removal of IRB Members
- SOP 111 Conflict of Interest
- SOP 112 Creation and Management of SOPs
- SOP 113 Data Management and Disposition
- SOP 115 Functions of the IRB
- SOP 117 Informed Consent & Assent Processes
- SOP 118 Inspections and Audits of Research Records
- SOP 119 International Research
- SOP 120 Disposition of IRB Records
- SOP 121 Quality Improvement Versus Research
- SOP 122 Administration of the IRB
- SOP 124 Review and Approval of Studies
- SOP 125 Safety and Monitoring
- SOP 126 Membership of the IRB
- SOP 128 Vulnerable Populations
- SOP 129 Required Reporting – Protocol violations, deviations and noncompliance
- SOP 130 IRB Approval with Conditions
- SOP 132 Public Data Sets
- SOP 133 Case Study/Case Series
- SOP 134 Required Reporting – Unanticipated Problems and Adverse Events
- SOP 135 Device Research – Significant Risk Versus Non-Significant Risk Determination
- SOP 138 Use of Students as Research Subjects
- SOP 139 Research Involving Deception or Incomplete Disclosure
- SOP 144 Source Documents in Human Subjects Research
- SOP 147 Public Health Practice versus Research
- SOP 148 Phlebotomy Qualifications in Human Subjects Research
- SOP 149 Engagement in Research with Human Subjects
- SOP 150 Research Subject to the Revised Common Rule
- SOP 151 External Research Requests
- SOP 152 Prep and Approval of IRB Meeting Minutes
- SOP 154 Suspensions and Terminations
Financial Conflicts of Interest in Funded Research
Human Research Protection Policy
OSA External Funding/Sponsored Project Proposal Submission Policy