IMPORTANT NOTICE: A new FDA rule will require consent forms for medical devices and drug trials to explain that data will be made public through an NIH website at http://www.ClinicalTrials.gov. This rule is effective March 7, 2011, and compliance to this rule is effective March 7, 2012. For more information about the rule, please click here.

The IRB requires all IRB documents be submitted through IRBNet. This includes the IRB proposal, modification requests, progress reports, and final reports. For the IRB proposal form or sample consent or assent forms, you must register on IRBNet. For information regarding registration, view the IRBNet Resources page on the left hand side.

Sample Consent/Assent Forms:

Consent Form - One

Consent Form - Two

Assent Form - One

Instructor Certification Form for Class Projects

Instructors/faculty of research courses that includes human subject research projects are required to fill out the Certification Form in order to act as the IRB for class projects.  These projects would be for class credit only and the results would not be for publication.  Instructors/faculty send the completed form to the IRB Administrator, DPL 101R, along with their CITI IRB Training Certificate. The certification form and CITI certificate can also be e-mailed to Kelly at kamclain@uaa.alaska.edu. The following link is to this form:

• Certification Form for Course Instructors/Faculty