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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

IRB Authority and Independence Policy
August 6, 2014
Review of Change of Protocols by Full IRB

Research with Coded Information and Specimens

Conflicts of Interest of Non-UW-Madison Key Personnel

Publication and Communication Policy

HRPP Compliance Monitoring and Quality Improvement

Continuing Review by Full IRB
Control of Test Articles Used in Research

Review of Data and Safety Monitoring in Research

Defining Human Subjects Research
Exceptions to Informed Consent Requirements in Emergency Situations

Emergency Use of Test Articles

Equitable Selection of Research Participants

Policy and Procedures for Exempt Research

Existing Datasets Policy

Expedited Review of Protocols

Use of Human Fetal Tissue in Research
December 11, 2014
Five Year Renewal Policy

Human Research Protection Program Advisory Committee Charter  
HRPP Education and Training Policy

Institutional Official in Charge of HRPP

Exception to Five Year Renewal Policy (HS IRBs)

Use of a Humanitarian Use Device (HUD) for Treatment or Research

Obtaining and Documenting Informed Consent

Initial Review of Research by Full IRB
IRB Authorization Agreements

IRB Composition Policy

IRB Consultants

IRB Meetings
December 11, 2014
IRB Purview December 11, 2014
Conflict of Interest Policy for Institutional Review Board Members and Consultants
 
Convened IRB Meeting Minutes  
Compliance with Human Research Protections in Sponsored Research  
Maintenance of IRB Records
 
Retention of IRB Records
 
IRB Roster Policy
 
Monitoring the Consent Process
 
Multisite Research Studies
 
Noncompliance Policy (Reporting Noncompliance and Handling Noncompliance Reports)
 
Recruitment of Research Participants
 
Principal Investigator Status for UW-Madison Human Subjects Protocols
 
Protecting Research Participants Privacy Interests and Confidentiality of Data
 
Provision of Sufficient IRBs
 
Qualifications of IRB Personnel
 
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 Subjects Lacking Capacity to Consent
 
Review of Research Involving Vulnerable Participants
 
Expert Review
December 11, 2014
Review of Research Involving Prisoners
 
IRB Review of Protocol Resources
 
Review of Social and Behavioral Science Protocols with Genetic Testing Component
 
Review of Test Article Research
 
IRB Analysis of Risks and Benefits of Research
 
Evaluating the Scientific or Scholarly Merits of Proposed Research  
Student Research: Policies and Guidelines
 
Suspension and Termination of Approved Research
 
Unanticipated Problems Policy
 



Keywords:human subjects research policies, research policy,   Doc ID:34101
Owner:Ryan M.Group:Office of the Vice Chancellor for Research and Graduate Education and Graduate School
Created:2013-10-02 14:42 CSTUpdated:2015-02-16 09:59 CST
Sites:Office of the Vice Chancellor for Research and Graduate Education and Graduate School
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