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Forms, Policies and Procedures

To the left is a separate link to the submission forms needed for the IRB process, a slide presentation that provides information on how to complete the New Protocol Form (Submission Form for Initial Review), and model/template/checklist documents to assist researchers in developing informed consent materials. Researchers are encouraged to review the Frequently Asked Questions (FAQs) as they provide answers that may facilitate the IRB process as well as discuss some of the duties of primary investigators who have achieved IRB approval for their studies.

Note: Effective August 31, 2010 the Manual for Research with Human Subjects, revision date 12/2009, has been retired from use and removed from our website.

IRB Policies and Procedures   Submission-Related Forms

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