Forms

All applications for IRB review should be submitted through the HawkIRB system. The HawkIRB system includes:

·         applications for new projects, modifications and continuing reviews,

·         forms for reporting unanticipated problems and adverse events (REFs)

·         consent templates (standard informed consent, VAMC informed consent, UIHC Record of Informed Consent, Assent, Spanish “short form” consent, consent as a letter)

·         project closure form

Consent forms, scripts, advertisements, and other materials can be uploaded to HawkIRB during your application.

The links on this page are to forms or instructions that are not available on the HawkIRB system but that you might be required to submit with your application.

 

IRB-related forms

Form (in alphabetical order) Use
Evaluation to Sign an Informed Consent This document could be used with cognitively impaired adults to assess ability to provide informed consent
Individual Investigator Agreement
(Federally funded research)		 For use with investigators unaffiliated with the UI where the UI IRB will be the IRB of record - Do not use this form without calling the HSO first!
Individual Investigator Agreement
(non-federally funded research)		 For use with investigators unaffiliated with the UI where the UI IRB will be the IRB of record - Do not use this form without calling the HSO first!
Protocol Outline This is a suggested outline for writing a protocol for a study that involves a clinical or therapeutic intervention.
Specimen/Data Repository Procedures at the UI To be used when setting up a formal specimen or data repository -- Call the HSO for more information.
Compensation Request Form To be used when obtaining information from subjects for the purpose of payment for their involvement in research. 

 If you have any problems or questions with any of the forms/templates, please contact the Human Subjects Office at 319-335-6564 or irb@uiowa.edu.