Full Board Category Review

How do I submit a new Full Board Review Research Project?

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Investigators seeking Full Board review complete and sign an IRB Application Form, and attach all appropriate documents relevant to that particular protocol well in time for review at the next meeting. IRB meeting schedule and deadline dates are listed elsewhere on this website.

Please submit all protocols to the Office of Research Compliance located in CBH Suite 160 during business hours (8 am - 5 pm).

Note that investigators must submit the appropriate amount of hard-copies for proper IRB review. No E-versions of research-related documents will be accepted.

New IRB Full Board Protocol:

(1) Signed Original of the IRB New Protocol Application

(2) Six (6) Copies of the following documents:

(3) Four (4) Copies of the following documents:

  • Federal grant application (if applicable)
  • Clinical Protocol (for Clinical Trials)
  • Investigator's Brochure (if applicable and for Clinical Trials
  • All Correspondence related to this protocol for the Sponsor

(4) One (1) Copy of the following documents:

  • Curriculum Vitae of Principal Investigator
  • Conflict of Interest (COI) for EACH listed key personnel on project
  • Certificate of Training for Human Subject Research (CITI) for EACH listed key personnel on project
This page last updated 17th Jun 2014