This session will provide new researchers with the basic skills to manage a study that will be submitted for expedited review.  Attendees will learn about the role and responsibilities of the IRB, submission and review process, and regulatory issues commonly encountered with minimal risk studies.

You should attend this session if you are involved in any social-behavioral research or biomedical studies that include non-invasive sampling or minor procedures such as MRI.  This session and the IRB 101 for Greater than Minimal Risk Studies contain similar introductory information.