To facilitate the design, regulatory approval, and conduct of clinically-based immunological research by CCTI investigators
To facilitate communication between immunologists and clinicians to build synergy and develop innovative hypotheses, immunologic studies and therapies involving human subjects
Services
Assistance with preparation of regulatory documents for the Institutional review Board (IRB)
Assistance with recruitment of subjects to participate in immunological studies
Coordination of human sample procurement
Organization of seminar series and other forums promoting communication between clinicians and immunologists to foster translational immunology research
