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Human Subjects Research Protection Program (HRPP) Policy Index

The HRPP maintains the human subjects research protections policies utilized by the UW-Madison Institutional Review Boards (IRBs) and campus officials. A list of these policies is below. Using the above search box is recommended when looking for specific policies.

Document
Version Date

Adequate Resources for Human Research Protection Program


Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Subjects Research Policy
August 6, 2014
Applying State Law in Human Research

Compliance with Human Research Protections in Sponsored Research

Conflict of Interest Policy for Institutional Review Board Members and Consultants

Conflicts of Interest of Non-UW-Madison Key Personnel

Continuing Review by Full IRB

Control of Test Articles Used in Research 

Cross-Campus Human Research Protection Program (HRPP) Committee Charter
September 1, 2014
Emergency Use of Test Articles
Engagement in Human Participants Research at UW-Madison 
March 26, 2015
Equitable Selection of Research Participants

Evaluating the Scientific or Scholarly Merits of Proposed Research
Exceptions to Informed Consent Requirements in Emergency Situations

Existing Datasets Policy 

Expedited Review of Protocols

Expert Review
December 11, 2014
Five Year Replacement/Renewal
March 26, 2015
HRPP Compliance Monitoring and Quality Improvement

HRPP Education and Training Policy

Initial Review of Research by Full IRB

Institutional Official in Charge of HRPP
IRB Analysis of Risks and Benefits of Research

IRB Authority and Independence
August 6, 2014
IRB Authorization Agreements

IRB Composition Policy

IRB Consultants
IRB Meeting Minutes and Regulatory Documentation
March 26, 2015
IRB Meetings
December 11, 2014
IRB of RecordMarch 26, 2015
IRB Purview 
December 11, 2014
IRB Review of Study Resources

IRB Roster Policy
Maintenance of IRB Records
 
Monitoring the Consent ProcessMarch 26, 2015
Noncompliance Policy (Reporting Noncompliance and Handling Noncompliance Reports)
 
Obtaining and Documenting Informed Consent
 
Policy and Procedures for Exempt Research
 
Principal Investigator Status for UW-Madison Human Participants Studies
 
Protecting Research Participants Privacy Interests and Confidentiality of Data
 
Provision of Sufficient IRBs
 
Publication and Communication Policy
 
Qualifications of IRB Personnel
 
Recruitment of Research Participants
 
Reporting Questions, Suggestions and Concerns about HRPP and IRBs
 
Reporting to Federal Authorities (Unanticipated Problems, Noncompliance and Suspensions and Terminations of Research)
 
Research with Adult Participants Lacking Capacity to Consent
March 26, 2015
Retention of IRB Records

Review of Change of Protocols by Full IRB
 
Review of Data and Safety Monitoring in Research

Review of Research Involving Vulnerable Participants
 
Review of Social and Behavioral Science Studies with Genetic Testing Component
 
Review of Test Article Research
 
Student Research
March 26, 2015
Study ClosureMarch 26, 2015
Suspension and Termination of Approved Research

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 15:42 CDTUpdated:2015-04-23 09:27 CDT
Sites:VCRGE and Graduate School
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