IRB Ongoing Review
Please use these forms for routine continuing review of a study (at least annually, or more frequent, as required by the IRB), or to submit a final report to the IRB for study closure.
If you have any questions about the Continuing Review Process please contact:
Please use these forms to report changes in the study (e.g., changes in protocol, changes in Informed Consent documents, amendments, etc.) including changes in staff assigned to conduct elements of the study.
If you have any questions please contact: