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Clinical Trial Routing Form (CTRF)

  • The Clinical Trial Routing Form (CTRF) allows study agreement contract negotiations to proceed in parallel with budget negotiations and regulatory approval.  The Clinical Trial Routing Form (CTRF) is typically required for all activity in 31200, Clinical Trial Site Activity and for investigator-initiated industry-sponsored clinical trials (in the Research class codes) when there is a draft agreement prior to a PAF routing.

    See ITS Clinical Trial Routing Forms Quick Reference Card teps to enter a Clinical Trial Routing Form (CTRF) in eRPM.