Our Mission
The Clinical Research Compliance Office (CRCO) was created in an effort to consolidate and initiate university-wide QA of human subjects research, strategic initiatives in the area of human subjects research and internal assessment and compliance with applicable regulations governing human subjects research.
Our Services:
- Develop and implement a clinical research compliance plan
- Track, investigate and respond to clinical research complaints and allegations
- Trend information and report
- Create education and training
- Develop corrective action plans
- Respond/coordinate responses to federal agencies (e.g. OHRP, FDA, VA, etc.)
- Conduct quality and compliance assessments for:
- Create education and training
- New research initiatives
- Existing internal clinical research compliance programs
- Oversee auditing program for:
