STANDARD OPERATING PROCEDURES (SOP)SOP (July 2023)-download pdfSOP Addendum (Oct 2020) - download pdf Table of Contents1: Human Research Protection Program2: Quality Assurance3: Education & Training4: Institutional Review Board5: Human Subject Research Determination6: Exempt Studies7: IRB Review Process8: Study Suspension, Termination and Investigator Hold9: Research overseen by a non-UVA IRB of Record 10: Documentation and Records11: Obtaining Informed Consent from Research Subjects12: Vulnerable Subjects in Research13: FDA-Regulated Research14: Reportable Events15: Unanticipated Problems Involving Risks to Subjects or Others16: Non-compliance17: Complaints18: Reporting to Regulatory Agencies and Organizational Officials19: Investigator Responsibilities20: Sponsored Research21: Conflict of Interest in Research22: Participant Outreach23: Health Insurance Portability and Accountability Act (HIPAA)24: Information Security25: Special Topic