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Request sIRB Documentation for Grant Application

If you’re planning to conduct a multisite clinical trial or cooperative research study funded by the National Institutes of Health (NIH) or other U.S. federal funding agency, you’ll need to identify the single IRB (sIRB) for your study as part of your grant application. Other funding agencies and organizations may have similar requirements.

Planning to rely on Advarra’s IRB? Use this form to request:

  • Letter of support: This document indicates Advarra is willing to serve as the IRB of record for the trial.
  • Communication plan: This document describes how communication between participating sites and the sIRB will take place.

Complete the form to request one or both of these documents.

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Certificate of Attendance

Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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