Regulatory Support – Institute for Clinical and Translational Research

The ICTR offers education, expert advice and resources to better equip study teams to conduct research that is ethical, relevant and responsive to the interests of patients and research participants.

ClinicalTrials.gov (CT.gov) Program

Guidance and support on CT.gov reporting and federal regulations.

Research Ethics Consultation

Advice and support for investigators as they address ethical questions that arise during study design and execution.

Drug and Device Resource Service (DDRS)

Resources needed to help manage the development and use of investigational drugs, biologics devices and software in clinical research.

Institutional Review Board (IRB)

Protects the rights and welfare of the human subjects participating in research conducted by faculty and staff at the Institutions.

Funded by the National Center for Advancing Translational Sciences through the Clinical & Translational Science Awards Program, grant number 1UM1TR004926-01.