The Human Research Protection Program (HRPP) provides oversight for all research activities involving human participants at the University of Wisconsin–Madison. The HRPP is a collective effort of all who participate in the conduct, review, approval, and facilitation of human participants research at UW–Madison. These groups work closely together to ensure the ethical, safe, and legal conduct of human research.

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The HRPP strives to uphold the highest ethical, safety, quality, and regulatory standards in research involving human participants at UW-Madison and its affiliates. The HRPP is also responsible for ensuring compliance with federal regulations, state laws, and institutional policies.

The HRPP:

  • promotes the welfare and rights of human research participants
  • facilitates excellence in human research, and
  • provides education, timely review, and comprehensive monitoring for human research projects.

To safeguard the rights and welfare of human research subjects, UW-Madison adheres to the principles of The Belmont Report, as described here.

As part of the HRPP, the Institutional Review Boards Office is home to two IRBs on campus. These IRBs review all human subject research protocols in accordance with applicable federal regulations, state laws, and local and university policies.

  • The Health Sciences IRB: Reviews research protocols involving medical interventions or procedures where medical expertise is required for evaluation.
  • The Minimal Risk Research IRB: Reviews research protocols that present minimal risk to subjects, including medical interventions or procedures requiring medical expertise or knowledge of the health care setting and human participants research occurring within the social and behavioral sciences.

News

Reminder: Guidance & Resources on Enrolling Non-English-Speaking Participants

April 15, 2025

Resources available include the IRB’s comprehensive guidance on enrolling non-English-speaking participants in research, UW Health Interpreter Services for faculty within SMPH and/or recruiting UW Health patients within UW Health facilities, and translated short forms.

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New Guidance: HCC/Non-HCC Collaborative Research

April 15, 2025

The Office of Compliance has published new guidance for study teams with members both within and outside the healthcare component (HCC).

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Stop Work Orders, Suspension of Work, or Funding Terminations  

April 3, 2025

If a researcher receives a directive from a federal funding agency to stop, pause, suspend, modify, or terminate activities on an award, investigators should consider whether a reportable event and/or change of protocol is necessary.

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Special Topics

Reliance & Navigation

The Reliance and Navigation Team (RELIANT) assists researchers with collaborative and multisite research issues and provides support to researchers in navigating institutional requirements.

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Toolkit Manuals

To supplement the Toolkit documents, the Investigator and Reliance Manuals are designed to guide you through policies and procedures related to the conduct of Human Research.

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Information for IRB Members

Resources to support IRB members in their reviews of research protocols.

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IRB Meeting Dates

Meeting dates for the Health Sciences and Minimal Risk Research IRB panels.

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IRB QI/Program Evaluation Self-Certification Tool

This tool is designed to help determine whether the project constitutes research or whether it is quality improvement or program evaluation.

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UW-Madison Science Hall pictured

Interested in Becoming an IRB Member?

We are looking for individuals interested in partnering with UW to protect the rights and welfare of our research participants by serving as an IRB member.

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