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