CSTR Institute Research Services

  • 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