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