1. All Campus Animal Planning and Advisory Committee Meeting Schedule
  2. Individual Conflict of Interest: Whom to Contact for Assistance
  3. HRPP Guidance, Forms and Resources
  4. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  5. Clinical Trials Registration & Results Reporting
  6. Academic Staff with Permanent PI Status
  7. Compliance Monitoring and Quality Improvement
  8. IRB Composition and Quality Performance
  9. Obtaining and Documenting Informed Consent
  10. IRB Members’ Conflicts of Interest
  11. UW–Madison SCRO Initial Review, Continuing Review, and Changes of Protocol Policy
  12. The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines
  13. Individual Financial Conflict of Interest: What to Report
  14. UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
  15. Frequently Asked Questions about Conflict of Interest
  16. Export Control Training Modules
  17. SCRO Protocol Submission
  18. Human Subjects Research Protection Program (HRPP) Policy Index
  19. Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
  20. Review of Research Involving Vulnerable Participants
  21. Recruitment of Research Participants Guidance
  22. Instructions for Linking Previous CITI Training to Your NetID
  23. Research with Adult Participants Lacking Capacity to Consent
  24. UW–Madison Office of Research Policy and Integrity Financial Conflict of Interest Policy and Procedures: Guidance Document
  25. Good Clinical Practice (GCP) Training Guidance and Instructions
  26. Instructions for Completing CITI Human Participants Research Training
  27. Research Participants
  28. I-129 Visa Certification Form
  29. Cross-Campus Human Research Protection Program (HRPP) Committee Charter
  30. Conflict of Interest Policy
  31. COI Committee: Evaluating Conflicts of Interest
  32. Post-Approval Monitoring Program
  33. Export Control Guidance Documents, Templates and Reports
  34. Issues in Human Subjects Research When State Law May Apply
  35. Obligations and Protections for Graduate Students and Postdoctoral Research Associates in Reporting Wrong Doing, Non-Compliance or Research Misconduct
  36. Misconduct in Scholarly Research
  37. Retention of IRB Records
  38. Continuing Review: Submission and Review
  39. Study Closure
  40. UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement
  41. USDA NIFA Capacity Fund (142) RCR Training Requirements
  42. USDA NIFA RCR Training Requirements
  43. University of Wisconsin – Madison Unmanned Aircraft Systems (UAS) Policy
  44. Reviewer's Tools
  45. Management Plan Notification Letter Example
  46. Sub-recipients for PHS Funded Research
  47. Contact Information for Reporting Suggestions and Concerns
  48. Conflict of Interest Training Course
  49. PI Status
  50. Request for Approval to Serve as PI
  51. Changes in Research Activities: Submission and Review
  52. Noncompliance
  53. HRPP Education and Training
  54. IRB Reliance
  55. HRPP Newsletter - Spring 2018
  56. Human Research Protection Program Newsletter
  57. Institutional Officials in Charge of HRPP
  58. Lab Close-Out Checklist
  59. Protecting Research Participants Privacy Interests and Confidentiality of Data
  60. Engagement in Human Participants Research at UW–Madison
  61. Evaluating the Scientific or Scholarly Merits of Proposed Research
  62. Equitable Selection of Research Participants Guidance
  63. Institutional Conflict of Interest Program
  64. Exempt Research
  65. Project Assessment Forms
  66. Certificate of Confidentiality (CoC) Application Help
  67. Authorship, Publication and Peer Review
  68. Responsible Conduct of Research
  69. UW–Madison Policy on Open Research & Free Interchange of Information
  70. Stem Cell Ethics and Policy Training
  71. Master List of Research Acronyms
  72. Stem Cell Research Oversight (SCRO) Committee Members
  73. UW-Madison Policy for Human Embryo and Human Pluripotent Stem Cell Research
  74. Office of Research Compliance and Office of Research Policy and Integrity Contacts
  75. Financial Conflict of Interest Management Plan Example
  76. Research Policy, Compliance, and Safety Training Courses
  77. Instructions for Completing CITI Refresher Training
  78. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  79. Creation and Dissemination of Policies and Related Documentation
  80. Procedure for Dealing with Misconduct in Scholarly Research
  81. Reporting Research Misconduct
  82. Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
  83. Exempt Research (for non-federally funded, non-FDA-regulated, non-VA research)
  84. De-Identified Publicly Available Datasets Guidance
  85. Reporting to Institutional and External Authorities
  86. Review of Data and Safety Monitoring in Research
  87. Maintenance of IRB Records
  88. ED/SBS IRB Principal Investigator Responsibilities
  89. PI Status for UW-Madison hESC Protocols
  90. Good Clinical Practice (GCP) Refresher Instructions
  91. UW-Madison Guidance for Investigators Requesting to Add hESC Lines to the UW-Madison hESC Registry
  92. UW-Madison Policy for Full Committee or Expedited Panel Review of Studies Using Human Embryo and or Human Pluripotent Stem Cells
  93. Preventing Noncompliance Guidance
  94. NIH Genomic Data Sharing Policy for Human Data Guidance
  95. IRB Meeting Minutes and Regulatory Documentation
  96. Exceptions to Informed Consent Requirements in Emergency Situations
  97. IRB Purview
  98. IRB Consultants Use and Conflict of Interest
  99. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  100. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  101. IRB Meetings
  102. Use of Human Fetal Tissue in Research
  103. IRB Analysis of Risks and Benefits of Research Guidance
  104. IRB Authority and Independence
  105. Conflicts of Interest of Non-UW-Madison Key Personnel
  106. HRPP and IRB Resources
  107. Suspension and Termination of Approved Research
  108. Campus IT Policies
  109. FDA IRB Regulations (21 CFR 56)
  110. List of Approved De-Identified Publicly Available Datasets
  111. Expert Review
  112. Reportable Abuse and Neglect Guidance
  113. Compliance with Human Research Protections in Sponsored Research
  114. OHRP Continuing Review Guidance
  115. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  116. UW-Madison HIPAA Program
  117. Unanticipated Problems
  118. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  119. Common Rule (45 CFR 46)
  120. Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
  121. Initial Review: Submission and Review Policy
  122. IRB Review of Study Resources
  123. Developing an Internal Quality Assurance (QA) Program Guidance
  124. Monitoring the Consent Process
  125. OHRP & FDA Expedited Review Guidance
  126. Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
  127. Considerations for Accepting or Ceding IRB Review Guidance
  128. ED/SBS IRB Office Guidance Index
  129. Use of Human Fetal Tissue in Research Policy Links
  130. Student Research
  131. Human Participants Research
  132. Post Approval Monitoring Program Services
  133. UW Post-Approval Monitors
  134. Bioethics Advisory Commitee on hESC Research
  135. UW-Madison SCRO Multisite Research Policy
  136. UW-Madison Guidance on Research involving the Creation of Human/Nonhuman Chimeras
  137. UW-Madison SCRO Committee Conflict of Interest Policy
  138. Mentor and Trainee Responsibilities
  139. Data Acquisition, Management, Sharing and Ownership
  140. Collaborative Research
  141. Conflict of Interest
  142. SCRO Committee: UW-Madison hESC Registry
  143. NIH Training Topics
  144. Institutional Conflict of Interest (ICOI) Procedures
  145. Institutional Conflict of Interest (ICOI) Policy
  146. Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
  147. Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
  148. University of Wisconsin-Madison Policy to Ensure that Federal Funds Are Not Expended for Unapproved Animal Research
  149. International Traffic in Arms Regulations (ITAR) FAQs
  150. Human Research Protection Program (HRPP) Newsletter - Spring 2017
  151. Principal Investigator (PI) Status
  152. Human Research Protection Program (HRPP) Newsletter - Fall 2016
  153. UW-Madison Export Control Organizational Structure
  154. UW-Madison Export Control Program Summary
  155. Human Research Protection Program (HRPP) Newsletter - Spring 2016
  156. WiCell UW-Madison Deposit Worksheet
  157. Biomaterial Addendum
  158. Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
  159. Export Control Compliance Program
  160. Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
  161. WISPER Export Control Process FAQ
  162. UW Human Research Protection Program Newsletter - Fall 2015
  163. Technology Control Plan