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