Standalone HIPAA Authorization template document, for use with the NCI CIRB Boilerplate ICF Template (version: 01/2021).

CIRB-approved boilerplate language (version: 09/2020), to be inserted into the CIRB-approved consent form(s) by the Investigator.

Template to report protocol deviations at the time of IRB Continuing Review.

Form to document study details when using an existing reliance agreement.

Form for use of the SMART IRB Master Agreement for federally funded cooperative research.

Local template reliance document for multisite studies not utilizing federal funding or existing agreements.

For completion when research will use or disclose the PHI of decedents.

For use in the event of unexpected enrollment of a non-English speaking subject.

Informed consent and HIPAA Authorization template document.

Assent template document for enrolling children ages 7-11 or 12-17.

Informed consent template document for research involving genetic testing.

A table for reporting adverse events to the IRB at the time of Continuing Review.