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Human Subjects Research Protection Program (HRPP) Policy Index

The HRPP maintains the human subjects research protections policies utilized by all UW–Madison Institutional Review Boards (IRBs) and campus officials. These policies are approved by the Cross-Campus HRPP Committee and a list is below. Using the above search box is recommended when looking for specific policies.

Additionally, researchers and study teams should review the documentation specific to the IRB office that they are working with. The Health Sciences IRBs Office hosts additional Policy and Guidance documents, while the Ed/SBS IRB Office hosts additional Guidance documents.

If you are unable to find what you are looking for on this page or the relevant IRB Office's pages, please visit the HRPP Guidance, Forms and Resources page, which contains forms, guidance documents, and links to other campus resources.

Document Version Date
Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy February 5, 2018
Changes in Research Activities: Submission and Review April 24, 2018
Compliance Monitoring and Quality Improvement May 3, 2019
Compliance with Human Research Protections in Sponsored Research March 1, 2012
Conflicts of Interest of Non-UW-Madison Key Personnel October 13, 2015
Continuing Review: Submission and Review August 15, 2018
Creation and Dissemination of Policies and Related Documentation July 7, 2015
Cross-Campus Human Research Protection Program (HRPP) Committee Charter August 23, 2017
Engagement in Human Participants Research at UW–Madison February 5, 2018
Evaluating the Scientific or Scholarly Merits of Proposed Research March 1, 2012
Exceptions to Informed Consent Requirements in Emergency Situations November 10, 2005
Exempt Research January 3, 2019
Expert Review December 11, 2014
HRPP and IRB Resources January 3, 2019
HRPP Education and Training January 3, 2019
Initial Review: Submission and Review Policy July 16, 2019
Institutional Official in Charge of HRPP January 3, 2019
IRB Authority and Independence January 3, 2019
IRB Composition and Quality Performance January 3, 2019
IRB Consultants Use and Conflict of Interest July 7, 2015
IRB Meeting Minutes and Regulatory Documentation February 5, 2018
IRB Meetings December 11, 2014
IRB Members’ Conflicts of Interest July 7, 2015
IRB Purview Just 16, 2019
IRB Reliance April 26, 2018
IRB Review of Study Resources August 28, 2015
Maintenance of IRB Records November 11, 2015
Monitoring the Consent Process March 26, 2015
Noncompliance January 3, 2019
Obtaining and Documenting Informed Consent May 2, 2019
Principal Investigator Status for UW–Madison Studies Involving Human Participants August 28, 2015
Protecting Research Participants Privacy Interests and Confidentiality of Data February 5, 2018
Reporting of Suggestions and Concerns Regarding HRPP Performance and Function January 3, 2019
Reporting of Suggestions and Concerns Regarding the Protection of Research Participants January 3, 2019
Reporting to Institutional and External Authorities August 28, 2015
Research with Adult Participants Lacking Capacity to Consent May 3, 2019
Retention of IRB Records August 15, 2018
Review of Data and Safety Monitoring in Research August 28, 2015
Review of Research Involving Vulnerable Participants February 5, 2018
Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy May 31, 2017
Student Research March 26, 2015
Study Closure August 15, 2018
Suspension and Termination of Approved Research January 3, 2019
Unanticipated Problems January 3, 2019
Use of Human Fetal Tissue in Research December 11, 2014



Keywords:human subjects research policies policy hrpp index   Doc ID:34101
Owner:Travis D.Group:VCRGE and Graduate School
Created:2013-10-02 15:42 CDTUpdated:2019-08-23 15:39 CDT
Sites:Health Sciences IRBs, VCRGE and Graduate School
Feedback:  3   4