ORO Checklists and Audit Tools
The Research Compliance Officer (RCO) Audit Tools below are provided as examples; RCOs are not required to use these specific forms or format. However, RCOs must audit, at a minimum, all the required information in the audit tools.
HRPP and RDC
Research and Development Committee (RDC) Checklist (February 2025)
Investigational Pharmacy Checklist (March 2015)
VHA Directive 1200.05 Checklist (February 2025)
Research Information Security
Research Information Security (RIS) Checklist (November 2024)
Research Safety and Animal Welfare
ACUP Checklist is currently being revised to reflect changes in requirements related to the recent issuance of VHA Directive 1200.07.
Research Safety and Security (RSSP) Checklist (May 2025)
Research Compliance and Technical Assistance
2025-26 ORO Guidance for RCO Auditing and Training Requirements
2025-26 Animal Welfare Regulatory Audit Tool
2025-26 HRP Regulatory Audit Tool
2025-26 Informed Consent Audit Tool
2025-26 Research Safety Regulatory Audit Tool
2025-26 Optional FDC Tracking Tool
Active Studies and Audit History Tracking Tool
Summary Report of RCO QA of Reportable Events Template
Flowchart for RCO IC Audit Requirements
Flowchart of RCO HRP Regulatory Audit Requirements