- Investigator initiated studies [Request a meeting with a facilitator]
- Help with assessing the feasibility of your study
- Guidance with budgets
- IRB applications (pre-review of protocol)
- Protocol development
- Clinical Trials and FDA studies
- Access to Research Compliance Offices
- Review of Research Protocol
- CITI (Human Subjects) Training
- Navigation support for protocol involving:
- Multiple IRBs
- Multiple IACUCs
- Good Laboratory Practices (GLPs)
- Investigational Drugs, Devices, Clinical Trials
- Ongoing Compliance & Research Management:
- HIPAA Compliance and Training
- Professional Development and Ethics courses
Translational Research Management Support Software
