Below are guidance documents, forms, and helpful links when relying on an external IRB.
Guidelines for Relying on an External IRB – Updated 3/18/16
Guidance for Relying on NCI CIRB – Updated 4/25/14
CIRB Approved Consent Boilerplate Language – Updated 3/30/16
CTTI Considerations – Considerations to Support Communication Between Institutions and Outside IRBs When Responsibilities are Being Assigned for Multicenter Clinical Trial Protocols