- SOP 001: Definitions
- SOP 002: Applicability of Regulations and Laws
- SOP 003: Routine Task
- SOP 004: Institutional Components and Authority
- SOP 010: Incoming Items Directed to the IRB
- SOP 011: Pre-Review
- SOP 012: Changes Required by the IRB to Secure Approval
- SOP 013: Reportable Information Items that are Potentially Problematic
- SOP 014: Investigations
- SOP 015: Suspension or Termination of IRB Approval
- SOP 016: Continuation of Subjects in Expired Research
- SOP 017: Post-Review
- SOP 018: Observation of the Consent Process
- SOP 019: Applying Flex Policies
- SOP 020: IRB Meeting Scheduling and Notification
- SOP 021: Consultation to the IRB
- SOP 022: IRB Meeting Preparation
- SOP 023: Conduct of IRB Meetings
- SOP 024: Conflicting Interersts of IRB Members
- SOP 025: IRB Meeting Attendance Monitoring
- SOP 026: IRB Meeting Minutes
- SOP 030: IRB Formation
- SOP 031: IRB Removal
- SOP 032: IRB Membership Addition
- SOP 033: IRB Membership Removal
- SOP 034: IRB Chair Designations
- SOP 040: Designated Reviewers
- SOP 041: Non-Committee Review Preparation
- SOP 042: Conduct of a Non-Committee Review
- SOP 043: Deferral of IRB Oversight
- SOP 050: Cognitively Impaired Adults, Legally Authorized Representatives, Children, and Guardians
- SOP 051: Emergency Use of a Test Article
- SOP 052: Emergency Use of a Test Article - Post Review
- SOP 053: Review of Research Not Otherwise Approvable
- SOP 054: External Exempt Reviewers
- SOP 060: Institutional Conflicts of Interest
- SOP 061: Financial Conflicts of Interest of Investigators and Research Staff
- SOP 070: IRB Records
- SOP 071: IRB Record Retention
- SOP 080: Evaluation of the Human Subjects Protection Program
- SOP 081: Process Improvement of the Human Subjects Protection Program
- SOP 082: Policy, Checklist, Template and/or Worksheet Creation and Update