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External IRB Authorization & Reliance AgreementMarch 4th, 2019
This Agreement does not preclude the Institution from participating in any other IRB authorization agreements that it may have or may enter into with other IRB(s) for human subject research other than the studies for which review is ceded to Advarra under this Agreement. This document must be kept on file by all parties and provided to the FDA, OHRP, and/or other applicable regulatory agencies upon request. This Agreement may be executed in any number of counterparts, either in original, portable document file (PDF) or faxed form.
