Part 1: Background and Overview Topics

Part 2: Organizing the Office

Part 3: Organizing the IRB Committee

Part 4: Review Categories

Part 5: Initial Protocol Review and The Full-Committee Meeting

Part 6: Informed Consent

Part 7: Continuing Review

Part 8: Administrative and Regulatory Issues

Part 9: Issues Based on Study Population

Part 10: IRB Issues Based on Study Design or Category