1. Human Subjects Research Protection Program (HRPP) Policy Index
  2. Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
  3. Review of Research Involving Vulnerable Participants
  4. Recruitment of Research Participants Guidance
  5. Instructions for Linking Previous CITI Training to Your NetID
  6. Research with Adult Participants Lacking Capacity to Consent
  7. UW–Madison Office of Research Policy and Integrity Financial Conflict of Interest Policy and Procedures: Guidance Document
  8. Good Clinical Practice (GCP) Training Guidance and Instructions
  9. Instructions for Completing CITI Human Participants Research Training
  10. HRPP Guidance, Forms and Resources
  11. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  12. Research Participants
  13. I-129 Visa Certification Form
  14. Cross-Campus Human Research Protection Program (HRPP) Committee Charter
  15. Academic Staff with Permanent PI Status
  16. Conflict of Interest Policy
  17. COI Committee: Evaluating Conflicts of Interest
  18. Export Control Training Modules
  19. Post-Approval Monitoring Program
  20. Export Control Guidance Documents, Templates and Reports
  21. Issues in Human Subjects Research When State Law May Apply
  22. Obligations and Protections for Graduate Students and Postdoctoral Research Associates in Reporting Wrong Doing, Non-Compliance or Research Misconduct
  23. Misconduct in Scholarly Research
  24. Retention of IRB Records
  25. Continuing Review: Submission and Review
  26. Study Closure
  27. Individual Conflict of Interest: Whom to Contact for Assistance
  28. UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement
  29. USDA NIFA Capacity Fund (142) RCR Training Requirements
  30. USDA NIFA RCR Training Requirements
  31. University of Wisconsin – Madison Unmanned Aircraft Systems (UAS) Policy
  32. Reviewer's Tools
  33. Management Plan Notification Letter Example
  34. Sub-recipients for PHS Funded Research
  35. UW–Madison SCRO Initial Review, Continuing Review, and Changes of Protocol Policy
  36. UW–Madison Federalwide Assurance (FWA)
  37. Frequently Asked Questions about Conflict of Interest
  38. The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines
  39. Individual Financial Conflict of Interest: What to Report
  40. Contact Information for Reporting Suggestions and Concerns
  41. Conflict of Interest Training Course
  42. All Campus Animal Care and Advisory Committee Meeting Schedule
  43. PI Status
  44. Request for Approval to Serve as PI
  45. Changes in Research Activities: Submission and Review
  46. Noncompliance
  47. HRPP Education and Training
  48. IRB Reliance
  49. HRPP Newsletter - Spring 2018
  50. Human Research Protection Program Newsletter
  51. SCRO Protocol Submission
  52. Institutional Officials in Charge of HRPP
  53. Lab Close-Out Checklist
  54. Protecting Research Participants Privacy Interests and Confidentiality of Data
  55. Engagement in Human Participants Research at UW–Madison
  56. Evaluating the Scientific or Scholarly Merits of Proposed Research
  57. Equitable Selection of Research Participants Guidance
  58. Institutional Conflict of Interest Program
  59. Exempt Research
  60. Project Assessment Forms
  61. Certificate of Confidentiality (CoC) Application Help
  62. Authorship, Publication and Peer Review
  63. Responsible Conduct of Research
  64. UW–Madison Policy on Open Research & Free Interchange of Information
  65. Stem Cell Ethics and Policy Training
  66. Master List of Research Acronyms
  67. Stem Cell Research Oversight (SCRO) Committee Members
  68. UW-Madison Policy for Human Embryo and Human Pluripotent Stem Cell Research
  69. Office of Research Compliance and Office of Research Policy and Integrity Contacts
  70. Financial Conflict of Interest Management Plan Example
  71. Fee for Service Agreement Template
  72. Research Ethics Courses Offered at UW–Madison
  73. Research Policy, Compliance, and Safety Training Courses
  74. Instructions for Completing CITI Refresher Training
  75. IRB Members’ Conflicts of Interest
  76. Obtaining and Documenting Informed Consent
  77. Clinical Trials Registration & Results Reporting
  78. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  79. Creation and Dissemination of Policies and Related Documentation
  80. Procedure for Dealing with Misconduct in Scholarly Research
  81. Reporting Research Misconduct
  82. Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
  83. Exempt Research (for non-federally funded, non-FDA-regulated, non-VA research)
  84. De-Identified Publicly Available Datasets Guidance
  85. IRB Composition and Quality Performance
  86. Reporting to Institutional and External Authorities
  87. Review of Data and Safety Monitoring in Research
  88. Maintenance of IRB Records
  89. ED/SBS IRB Principal Investigator Responsibilities
  90. PI Status for UW-Madison hESC Protocols
  91. Good Clinical Practice (GCP) Refresher Instructions
  92. UW HRPP Quality Assurance
  93. UW-Madison Guidance for Investigators Requesting to Add hESC Lines to the UW-Madison hESC Registry
  94. UW-Madison Policy for Full Committee or Expedited Panel Review of Studies Using Human Embryo and or Human Pluripotent Stem Cells
  95. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  96. Common Rule (45 CFR 46)
  97. Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
  98. Initial Review: Submission and Review Policy
  99. List of Approved De-Identified Publicly Available Datasets
  100. Expert Review
  101. Reportable Abuse and Neglect Guidance
  102. Compliance with Human Research Protections in Sponsored Research
  103. OHRP Continuing Review Guidance
  104. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  105. UW-Madison HIPAA Program
  106. Unanticipated Problems
  107. Student Research
  108. Human Participants Research
  109. IRB Review of Study Resources
  110. Developing an Internal Quality Assurance (QA) Program Guidance
  111. Monitoring the Consent Process
  112. OHRP & FDA Expedited Review Guidance
  113. Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
  114. Considerations for Accepting or Ceding IRB Review Guidance
  115. ED/SBS IRB Office Guidance Index
  116. Use of Human Fetal Tissue in Research Policy Links
  117. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  118. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  119. Preventing Noncompliance Guidance
  120. NIH Genomic Data Sharing Policy for Human Data Guidance
  121. Compliance Monitoring and Quality Improvement
  122. IRB Meeting Minutes and Regulatory Documentation
  123. Exceptions to Informed Consent Requirements in Emergency Situations
  124. IRB Purview
  125. IRB Consultants Use and Conflict of Interest
  126. Campus IT Policies
  127. FDA IRB Regulations (21 CFR 56)
  128. IRB Meetings
  129. Use of Human Fetal Tissue in Research
  130. IRB Analysis of Risks and Benefits of Research Guidance
  131. IRB Authority and Independence
  132. Conflicts of Interest of Non-UW-Madison Key Personnel
  133. HRPP and IRB Resources
  134. Suspension and Termination of Approved Research
  135. Quality Assurance Committees
  136. Post Approval Monitoring Program Services
  137. UW Post-Approval Monitors
  138. Bioethics Advisory Commitee on hESC Research
  139. UW-Madison SCRO Multisite Research Policy
  140. UW-Madison Guidance on Research involving the Creation of Human/Nonhuman Chimeras
  141. UW-Madison SCRO Committee Conflict of Interest Policy
  142. Mentor and Trainee Responsibilities
  143. Data Acquisition, Management, Sharing and Ownership
  144. Collaborative Research
  145. Conflict of Interest
  146. SCRO Committee: UW-Madison hESC Registry
  147. NIH Training Topics
  148. Institutional Conflict of Interest (ICOI) Procedures
  149. Institutional Conflict of Interest (ICOI) Policy
  150. Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
  151. Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
  152. University of Wisconsin-Madison Policy to Ensure that Federal Funds Are Not Expended for Unapproved Animal Research
  153. International Traffic in Arms Regulations (ITAR) FAQs
  154. Human Research Protection Program (HRPP) Newsletter - Spring 2017
  155. Principal Investigator (PI) Status
  156. Human Research Protection Program (HRPP) Newsletter - Fall 2016
  157. UW-Madison Export Control Organizational Structure
  158. UW-Madison Export Control Program Summary
  159. Human Research Protection Program (HRPP) Newsletter - Spring 2016
  160. WiCell UW-Madison Deposit Worksheet
  161. Biomaterial Addendum
  162. Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
  163. Export Control Compliance Program
  164. Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
  165. WISPER Export Control Process FAQ
  166. UW Human Research Protection Program Newsletter - Fall 2015
  167. Technology Control Plan