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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. 

Version Date
Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
August 6, 2014
Changes in Research Activities: Submission and Review July 7, 2015
Compliance Monitoring and Quality Improvement August 28, 2015
Compliance with Human Research Protections in Sponsored Research
Conflicts of Interest of Non-UW-Madison Key Personnel October 13, 2015
Continuing Review: Submission and Review July 7, 2015
Control of Test Articles Used in Research
Creation and Dissemination of Policies and Related Documentation July 7, 2015
Cross-Campus Human Research Protection Program (HRPP) Committee Charter September 29, 2015
Emergency Use of Test Articles
Engagement in Human Participants Research at UW-Madison March 26, 2015
Evaluating the Scientific or Scholarly Merits of Proposed Research
Exceptions to Informed Consent Requirements in Emergency Situations
Exempt Research August 28, 2015
Expert Review December 11, 2014
Five Year Replacement/Renewal March 26, 2015
HRPP and IRB Resources August 28, 2015
HRPP Education and Training October 13, 2015
Initial Review: Submission and Review Policy July 7, 2015
Institutional Officials in Charge of HRPP July 7, 2015
IRB Authority and Independence August 6, 2014
IRB Composition and Quality Performance August 28, 2015
IRB Consultants Use and Conflict of Interest July 7, 2015
IRB Meeting Minutes and Regulatory Documentation March 26, 2015 
IRB Meetings December 11, 2014
IRB Members’ Conflicts of Interest July 7, 2015
IRB of Record March 26, 2015
IRB Purview December 11, 2014
IRB Review of Study Resources August 28, 2015
Maintenance of IRB Records  
Monitoring the Consent Process March 26, 2015
Noncompliance October 13, 2015
Obtaining and Documenting Informed Consent
Principal Investigator Status for UW-Madison Studies Involving Human Participants August 28, 2015
Protecting Research Participants Privacy Interests and Confidentiality of Data
Reporting of Suggestions and Concerns Regarding HRPP Performance and Function August 28, 2015
Reporting of Suggestions and Concerns Regarding the Protection of Research Participants August 28, 2015
Reporting to Institutional and External Authorities August 28, 2015
Research with Adult Participants Lacking Capacity to Consent March 26, 2015
Retention of IRB Records  
Review of Data and Safety Monitoring in Research August 28, 2015 
Review of Research Involving Vulnerable Participants  
Review of Test Article Research
Student Research March 26, 2015
Study Closure March 26, 2015
Suspension and Termination of Approved Research October 13, 2015
Unanticipated Problems Policy  
Use of a Humanitarian Use Device (HUD) for Treatment or Research  
Use of Human Fetal Tissue in Research
December 11, 2014

Keywords:human subjects research policies, research policy,   Doc ID:34101
Owner:Ryan M.Group:VCRGE and Graduate School
Created:2013-10-02 14:42 CSTUpdated:2015-11-19 09:34 CST
Sites:VCRGE and Graduate School
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