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