Below are guidance documents, forms, and helpful links when relying on an external IRB.
Guidelines for Relying on an External IRB – Updated 4/14/17
Guidance for Relying on NCI CIRB – Updated 6/1/17
CIRB Approved Consent Boilerplate Language – Updated 8/10/17
CTTI Considerations – Considerations to Support Communication Between Institutions and Outside IRBs When Responsibilities are Being Assigned for Multicenter Clinical Trial Protocols