The mission of the Research Regulatory Consultation group is twofold: 1) to Optimize Research Infrastructure and Regulatory Support Services for IIMS; and 2) to Optimize Safety and Protect the rights of Research Subjects participating in Clinical Research.

The services we offer to accomplish our mission are:

• To ensure processes efficiently support the ethical conduct of research to include safety monitoring of research subjects participating in clinical research.
• To serve as liaisons to investigators, research staff, research subjects, and research administration of the HSC.
• To identify and address choke points in research protocol and contract submission and approval processes.
• To develop and enhance the educational opportunities on research regulatory requirements for research investigators, team members, and administrators.
• To assist in development of a variety of agreements with external partners for general research areas and or specific research projects of mutual interest.

See our Staff listing for contact information.