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