The Office of Research Compliance is committed to helping faculty, staff, and students comply with all applicable federal, state, and institutional requirements and policies. Research compliance areas covered by this office include Human Subjects Protections, Animal Welfare, Biosafety and Conflict of Interest. These pages will provide information on policies and procedures, guidelines, educational programs, and monitoring and accountability in these areas.
The WVU Institutional Review Board (IRB) for the Protection of Human Research Subjects has moved to electronic submission of all forms. We can no longer accept hard copies since the only changes the electronic system can process are those that are submitted by the investigator. Please refer to our IRB Protocol Submission and Forms link for more information on the BRAAN 2 Electronic Submission System.
NOTICES!!
Effective Immediately – We are no longer offering the Human Research Ethics, HIPAA Research Requirements, and Good Clinical Practice Training modules on our website. CITI Training is now required.
BRAAN II Training Sessions
- None at this time.
Introduction to Good Clinical Practice Lectures
- Clinical Trial Process Presentation
- Not research, exempt, or expedited research
- Privacy and Confidentiality, Feb 08
- Investigator-Initiated, Pharma-Sponsored Clinical Trials in Human Subjects
