The CTSI offers detailed guidance for every step of the clinical research process.
To request CTSI services and support, please complete the CTSI Service Request Form.
Access the eIRB
The IRB requires that all human subject applications, amendments, and notifications be submitted through the eIRB system.
Learn more about accessing and using the eIRB.
Clinical Trial Facilitation
The CTSI provides expertise on protocol development, the IRB, and other regulatory concerns at $78 per hour.
For more information, please contact Selvin Ohene at firstname.lastname@example.org.