Skip to main content.

Flexible IRB Review

In November 2018, the KUMC Human Research Protection Program (HRPP) implemented a new policy for flexible IRB review. Flexible IRB review means a review and oversight process that applies human subjects protections commensurate with risk while reducing administrative burdens for researchers and the IRB. Flexible IRB review allows abbreviated IRB applications and consent forms, streamlined review by IRB Chair or staff members and elimination of the continuing review requirement. IRB SOP 20: Flexible IRB Review provides detailed information.

What types of research can be reviewed under Flexible Review?
The minimal risk research covered by the Flexible IRB Review policy includes:

  • Behavioral activities;
  • Analysis of data or specimens; and,
  • Biomedical studies

What are the eligibility criteria?
Research eligible for flexible review must meet three basic criteria:

  1. Minimal risk. Minimal risk means the probability and magnitude of harm or discomfort anticipated in the research are not greater in and of themselves than those ordinarily encountered in daily life or during the performance of routine physical or psychological examinations or tests.
  2. Does not involve federal funding or support. Federal funding or support is defined as: 
    • Funded by a direct federal grant
    • Funded through a sub-award or pilot grant associated with federal dollars
    • Includes personnel on a federally-funded training grant 
    • Research conducted under a no-cost extension
    • Data will be used to support a pending grant application or application for FDA approval (e.g., data collection in response to a scored grant submission with plans to re-submit)
    • Involves delivery of an FDA-regulated product or dietary supplement
    • Involves data collection about FDA-regulated products
    • Conducted under a contract that requires the investigator to adhere to federal human subjects regulations (e.g., 45 CFR 46, 34 CFR 97 or other references to the HHS Common Rule)
    • Involves any services that could be billed to a federal program
  3. Does not involve reliance on KUMC's IRB by collaborating institutions or organizations that apply federal regulations to all research regardless of funding source.

How do I request Flexible IRB Review for my project?
Requests for Flexible IRB Review are made in the electronic IRB submission system, using a special application form specifically designed for this type of review. Required documents include:

  • Project Description form
  • Study protocol
  • Information sheets or consent forms using the specific templates designed for Flexible Review
  • Data collection sheets, scripts, recruitment materials and other study documents

How is informed consent different under Flexible IRB Review?
Because federal regulations do not apply to research conducted under flexible review, information sheets and consent form documents can be significantly shortened and streamlined. In certain circumstances, signature requirements can be waived.

Please refer to IRB SOP 20 (section 20.6) to review Informed Consent Elements for Flexible IRB Review.
In addition, the KUMC HRPP developed several templates for studies that qualify for flexible review bulleted below. These templates can be found on the forms and template page here

  • Flexibility Info Sheet - Survey with Identifiable Information
  • Flexibility Info Sheet - Focus Group, no HIPAA
  • Flexibility Consent form - Focus Group with HIPAA
  • Flexibility Consent form - Registry
  • Flexibility Consent form - Biorepository
  • Flexibility Consent form - Minimal risk procedures

What are my responsibilities during the conduct of the research?
Regardless of funding source or type of review, investigators remain responsible for ethical conduct in research and for compliance with KUMC policies. Additional responsibilities under the policy for Flexible IRB Review include:

  • Immediately notify the IRB office if federal funding or support is obtained for the research or if any other of the eligibility criteria change during the study
  • Submit changes to the study design, study personnel or information sheets/consent documents for IRB review and approval
  • Report unanticipated problems as instructed on the Reportable Events webpage 
  • Close the study in the eIRB system at the time of completion

For additional questions about Flexible IRB Review, please contact

Research Administration

University of Kansas Medical Center
Research Administration
Mailstop 1039
3901 Rainbow Boulevard
Kansas City, KS 66160
Office Location: Support Services Building, Suite 120
Phone: 913-588-1261
Fax: 866-255-2129