1. Human Subjects Research Protection Program (HRPP) Policy Index
  2. Frequently Asked Questions about Conflict of Interest
  3. Biomaterial Addendum
  4. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  5. Individual Conflict of Interest: Whom to Contact for Assistance
  6. Post Approval Monitoring Program Services
  7. Clinical Trials Registration & Results Reporting
  8. UW–Madison United States Department of Agriculture (USDA) National Institute of Food and Agriculture (NIFA) Responsible Conduct of Research (RCR) Training Requirements
  9. Engagement in Human Participants Research at UW–Madison
  10. UW Human Research Protection Program Newsletter - Fall 2015
  11. Good Clinical Practice (GCP) Training Guidance and Instructions
  12. Human Research Protection Program (HRPP) Newsletter - Spring 2016
  13. Human Research Protection Program (HRPP) Newsletter - Fall 2016
  14. Human Research Protection Program Newsletter
  15. Good Clinical Practice (GCP) Refresher Instructions
  16. All Campus Animal Planning and Advisory Committee Meeting Schedule
  17. Certificate of Confidentiality (CoC) Application Help
  18. UW–Madison Office of Research Policy and Integrity Financial Conflict of Interest Policy and Procedures: Guidance Document
  19. IRB Meeting Minutes and Regulatory Documentation
  20. Changes in Research Activities: Submission and Review
  21. Stem Cell Research Oversight (SCRO) Committee Members
  22. HRPP Guidance, Forms and Resources
  23. Financial Conflict of Interest Management Plan Example
  24. Instructions for Completing CITI Refresher Training
  25. The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines
  26. Unmanned Aircraft System (UAS) Pilot Guidance
  27. Instructions for Linking Previous CITI Training to Your NetID
  28. Academic Staff with Permanent PI Status
  29. Use of Human Fetal Tissue in Research
  30. Compliance with Human Research Protections in Sponsored Research
  31. Monitoring the Consent Process
  32. Exceptions to Informed Consent Requirements in Emergency Situations
  33. IRB Meetings
  34. Contact Information for Reporting Suggestions and Concerns
  35. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  36. Institutional Conflict of Interest Program
  37. Research Vehicle Safety Oversight (RVSO)
  38. Individual Financial Conflict of Interest: What to Report
  39. Guidance for Data Management
  40. Autonomous Vehicle Guidance
  41. Guidance for Unammed Aircraft Systems Registration and Insurance
  42. Aircraft Guidance
  43. UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
  44. Institutional Conflict of Interest (ICOI) Procedures
  45. Institutional Conflict of Interest (ICOI) Policy
  46. UW-Madison Policy for Human Embryo and Human Pluripotent Stem Cell Research
  47. Initial Review: Submission and Review Policy
  48. IRB Purview
  49. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  50. Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
  51. Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
  52. Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
  53. Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
  54. Authorship, Publication and Peer Review
  55. Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
  56. UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement
  57. NIH Training Topics
  58. Compliance Monitoring and Quality Improvement
  59. Lab Close-Out Checklist
  60. Research with Adult Participants Lacking Capacity to Consent
  61. Obtaining and Documenting Informed Consent
  62. UW–Madison Stem Cell Research Oversight Guidance for Documentation of Provenance
  63. UW Post-Approval Monitors
  64. UW HRPP Quality Assurance
  65. Chain of Custody Template
  66. Exempt Research
  67. Quality Assurance Committees
  68. HRPP and IRB Resources
  69. Institutional Official in Charge of HRPP
  70. IRB Authority and Independence
  71. IRB Composition and Quality Performance
  72. Noncompliance
  73. Unanticipated Problems
  74. Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
  75. Suspension and Termination of Approved Research
  76. HRPP Education and Training
  77. IRB Members’ Conflicts of Interest
  78. UW–Madison SCRO Initial Review, Continuing Review, and Changes of Protocol Policy
  79. Export Control Training Modules
  80. SCRO Protocol Submission
  81. Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
  82. Review of Research Involving Vulnerable Participants
  83. Recruitment of Research Participants Guidance
  84. Instructions for Completing CITI Human Participants Research Training
  85. Research Participants
  86. I-129 Visa Certification Form
  87. Cross-Campus Human Research Protection Program (HRPP) Committee Charter
  88. Conflict of Interest Policy
  89. COI Committee: Evaluating Conflicts of Interest
  90. Post-Approval Monitoring Program
  91. Export Control Guidance Documents, Templates and Reports
  92. Issues in Human Subjects Research When State Law May Apply
  93. Obligations and Protections for Graduate Students and Postdoctoral Research Associates in Reporting Wrong Doing, Non-Compliance or Research Misconduct
  94. Misconduct in Scholarly Research
  95. Retention of IRB Records
  96. Continuing Review: Submission and Review
  97. Study Closure
  98. Reviewer's Tools
  99. Management Plan Notification Letter Example
  100. Sub-recipients for PHS Funded Research
  101. Conflict of Interest Training Course
  102. PI Status
  103. Request for Approval to Serve as PI
  104. IRB Reliance
  105. HRPP Newsletter - Spring 2018
  106. Protecting Research Participants Privacy Interests and Confidentiality of Data
  107. Evaluating the Scientific or Scholarly Merits of Proposed Research
  108. Equitable Selection of Research Participants Guidance
  109. Project Assessment Forms
  110. Responsible Conduct of Research
  111. UW–Madison Policy on Open Research & Free Interchange of Information
  112. Stem Cell Ethics and Policy Training
  113. Office of Research Compliance and Office of Research Policy and Integrity Contacts
  114. Research Policy, Compliance, and Safety Training Courses
  115. Creation and Dissemination of Policies and Related Documentation
  116. Procedure for Dealing with Misconduct in Scholarly Research
  117. Reporting Research Misconduct
  118. De-Identified Publicly Available Datasets Guidance
  119. Reporting to Institutional and External Authorities
  120. Review of Data and Safety Monitoring in Research
  121. Maintenance of IRB Records
  122. ED/SBS IRB Principal Investigator Responsibilities
  123. PI Status for UW-Madison hESC Protocols
  124. UW-Madison Guidance for Investigators Requesting to Add hESC Lines to the UW-Madison hESC Registry
  125. UW-Madison Policy for Full Committee or Expedited Panel Review of Studies Using Human Embryo and or Human Pluripotent Stem Cells
  126. Conflicts of Interest of Non-UW-Madison Key Personnel
  127. Reportable Abuse and Neglect Guidance
  128. Use of Human Fetal Tissue in Research Policy Links
  129. Student Research
  130. Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
  131. Human Participants Research
  132. Developing an Internal Quality Assurance (QA) Program Guidance
  133. UW-Madison HIPAA Program
  134. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  135. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  136. IRB Analysis of Risks and Benefits of Research Guidance
  137. Preventing Noncompliance Guidance
  138. Considerations for Accepting or Ceding IRB Review Guidance
  139. Campus IT Policies
  140. FDA IRB Regulations (21 CFR 56)
  141. IRB Review of Study Resources
  142. IRB Consultants Use and Conflict of Interest
  143. List of Approved De-Identified Publicly Available Datasets
  144. Expert Review
  145. NIH Genomic Data Sharing Policy for Human Data Guidance
  146. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  147. Common Rule (45 CFR 46)
  148. Bioethics Advisory Commitee on hESC Research
  149. UW-Madison SCRO Multisite Research Policy
  150. UW-Madison SCRO Committee Conflict of Interest Policy
  151. Mentor and Trainee Responsibilities
  152. Data Acquisition, Management, Sharing and Ownership
  153. Collaborative Research
  154. Conflict of Interest
  155. SCRO Committee: UW-Madison hESC Registry
  156. International Traffic in Arms Regulations (ITAR) FAQs
  157. Human Research Protection Program (HRPP) Newsletter - Spring 2017
  158. Principal Investigator (PI) Status
  159. UW-Madison Export Control Program Summary