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Plan ahead! The IRO has pre-released these forms to support applications under the 2018 requirements of the revised Common Rule (45 CFR 46).

Use these versions for all research studies to be approved by the IRB on or after January 21, 2019.

 

To see the version changes to these forms, visit https://extranet.fredhutch.org/en/u/iro/updates/11-19-2018.html.

Main Applications


Interventional Research

Use this form to apply for Institutional Review Board review of an interventional research study involving human subjects.

* View Word doc Last Updated | 12-11-18 10:31 p.m.

Observational Research

Use this form to apply for Institutional Review Board review of an observational research study involving human subjects.

* View Word doc Last Updated | 12-11-18 10:31 p.m.

Human Specimens or Data Research

Use this form to apply for Institutional Review Board review of a research study involving human specimens or data.

* View Word doc Last Updated | 12-11-18 10:31 p.m.

Supplements


Participating Site Application

This form should be used to obtain approval for a participating site outside the Fred Hutch/UW Cancer Consortium that relies on Fred Hutch IRB. Submit once IRB approval for the master file has been obtained.

* View Word doc Last Updated | 12-11-18 10:31 p.m.

Exempt Checklist

Use this if you qualify for an exemption from the requirement to obtain an IRB review.

* View Word doc Last Updated | 12-11-18 10:31 p.m.

Waiver of Consent Supplement

Use this form to request a full or partial waiver of consent for a research study.

* View Word doc Last Updated | 12-11-18 10:31 p.m.