Final Reports and Continuing Reviews

The IRB is required by 45 CFR 46.109(e) to conduct a continuing review of every "minimal risk or deception" IRB-approved protocol. At the time of Initial Approval, the IRB will inform the researcher(s) when Interim and/or Final Reports are due.

The IRB Administrator will send you an Annual Progress Report form each year, until your study is completed, and/or a Final Report form after completion of the study.