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Request sIRB Documentation for Grant Application

If you’ll be conducting a multisite clinical trial or cooperative research study funded by the NIH or other U.S. federal funding agency, your grant application must identify the study’s single IRB (sIRB).

Other funding agencies and organizations may have similar requirements.

Use this form to request these commonly required documents:

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

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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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