The standard turnaround time for review of a new protocol and informed consent (IC) for a single-site study is about 5 business days.
This allows time for administrative processing and circulation to the IRB for review, and 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 business 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.