The turnaround time expectation for review of a new protocol and informed consent (IC) is about 10 business days for multisite studies and 5 business days for single-site studies.
This allows time for administrative processing and circulation to the IRB for review, and time after the IRB meeting for preparation and transmission of study documents to the submitting party.
You will receive an e-mail notice of the outcome of the IRB’s review within 1 day of the IRB meeting.
Please note: Turnaround time is dependent upon complete and accurate submission of study documents, and may be extended if the IRB, upon review, requires further information.
For more information, please review our key Turnaround Times.