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