IRB Policies & Guidance

UI IRB Policies and Procedures

Guide to Human Subjects Protections in Research 

Guide to Human Subjects Protections in Research with Track Changes (revised April 2009)

Institutional Review Board Standard Operating Procedures 

UI IRB SOP with Track Changes (revised April 2009)

You can view a PDF file using Adobe Acrobat Reader. For information about how to download a version of Adobe Acrobat, visit their website at http://www.adobe.com/.

If you have any difficulties accessing these documents, please give us a call at 335-6564.

Policy Memorandums

IND/Outside Safety Reports Memo

Forms Not Available on HawkIRB

Click here for forms and/or instructions that are not available on the HawkIRB system but that you might be asked to submit with your application.

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, Record of Consent, Assent, consent as a letter, Spanish "short form" consent),
  • project closure forms

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

Other UI Policies and Guidance

Research Subject Payment -- U of I Policy and Procedures -- Revised 8.13.09

Cash Handling Policy - U of I Policy -- Revised 8.13.09 
Note: University Cash Handling Policies and Procedures apply when the type of research subject compensation is made using cash, gift certificates, personal property or any other item of value.  As described in the policy, all University of Iowa units and staff handling these types of payments are required to undergo the departmental and staff certification process. 

August 1, 2008 rollout of new policy and procedures - This rollout contains information on policy regarding the use of Social Security Numbers, the new record of consent template, listing of research team members on the informed consent document, medical record access for sponsor monitors, clarification that the informed consent can not be used as a data collection tool, a revised IRB definition of serious noncompliance, informed consent template language for pregnancy testing in the minor subject population, template letter examples and tips for effective recruitment, and information on VA CITI certification.