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Informed Consent
Use the templates below to construct Informed Consent form(s) for your participants to sign. Be sure to include your Informed Consent form(s) with your initial application. For internet research, please make sure your informed consent includes all of the elements in the Informed Consent Document for Adults (below). See the Informed Consent Process for more information.

Informed Consent Document for Adults (ages 18 and up)
Parental Informed Consent Document
Child (under13) Assent Document
Minor (ages 13-17) Assent Document

SPANISH VERSIONS:

SPANISH Informed Consent Document for Adults (ages 18 and up)
SPANISH Parental Informed Consent Document
SPANISH Child (ages 0-12) Assent Document
SPANISH Minor (ages 13-17) Assent Document

If you are doing INTERNET research or you are choosing not to use the NAU informed consent template, please see the Informed Consent Essential Information.

Amendments and Continuing Review

Research Amendment Form Submit this form to report changes or additions to an IRB approved project.

Application for Continuing Review Submit this form 30 days prior to the expiration of your approval if your research was approved under Expedited or Full Board review.

Adverse Events

Download and fill out the Adverse Reaction or Event Reporting Form to inform the IRB of any adverse events within 24 hours of the occurance.