1. Policy Updates and Announcements - 2014 - Individual Development Plans (IDPs)
  2. Changes in Research Activities: Submission and Review
  3. Noncompliance
  4. HRPP Education and Training
  5. Academic Staff with Permanent PI Status
  6. Continuing Review: Submission and Review
  7. IRB Reliance
  8. PI Status
  9. Instructions for Completing CITI Human Participants Research Training
  10. Instructions for Linking Previous CITI Training to Your NetID
  11. Human Subjects Research Protection Program (HRPP) Policy Index
  12. HRPP Newsletter - Spring 2018
  13. Human Research Protection Program Newsletter
  14. Frequently Asked Questions about Conflict of Interest
  15. SCRO Protocol Submission
  16. Reviewer's Tools
  17. Individual Conflict of Interest: Who to Contact for Assistance
  18. Institutional Officials in Charge of HRPP
  19. USDA NIFA Capacity Fund (142) RCR Training Requirements
  20. USDA NIFA RCR Training Requirements
  21. UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement
  22. The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines
  23. Export Control Training Modules
  24. Lab Close-Out Checklist
  25. Protecting Research Participants Privacy Interests and Confidentiality of Data
  26. Engagement in Human Participants Research at UW–Madison
  27. UW–Madison Federalwide Assurance (FWA)
  28. Evaluating the Scientific or Scholarly Merits of Proposed Research
  29. Equitable Selection of Research Participants Guidance
  30. Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
  31. Institutional Conflict of Interest Program
  32. Exempt Research
  33. Project Assessment Forms
  34. Certificate of Confidentiality (CoC) Application Help
  35. Authorship, Publication and Peer Review
  36. Responsible Conduct of Research
  37. UW–Madison Policy on Open Research & Free Interchange of Information
  38. Issues in Human Subjects Research When State Law May Apply
  39. Stem Cell Ethics and Policy Training
  40. Misconduct in Scholarly Research
  41. Post-Approval Monitoring Program
  42. Master List of Research Acronyms
  43. Good Clinical Practice (GCP) Training Guidance and Instructions
  44. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  45. Stem Cell Research Oversight (SCRO) Committee Members
  46. UW-Madison Policy for Human Embryo and Human Pluripotent Stem Cell Research
  47. Office of Research Compliance and Office of Research Policy and Integrity Contacts
  48. Financial Conflict of Interest Management Plan Example
  49. Human Participants Research Training
  50. UW–Madison Office of Research Policy and Integrity Financial Conflict of Interest Policy and Procedures: Guidance Document
  51. Recruitment of Research Participants Guidance
  52. Fee for Service Agreement Template
  53. Review of Research Involving Vulnerable Participants
  54. Research Ethics Courses Offered at UW–Madison
  55. HRPP Guidance, Forms and Resources
  56. Conflict of Interest Training Course
  57. Research Policy, Compliance, and Safety Training Courses
  58. Instructions for Completing CITI Refresher Training
  59. IRB Members’ Conflicts of Interest
  60. Export Control Guidance Documents, Templates and Reports
  61. Individual Financial Conflict of Interest: What to Report
  62. Obtaining and Documenting Informed Consent
  63. Clinical Trials Registration & Results Reporting
  64. University of Wisconsin – Madison Unmanned Aircraft Systems (UAS) Policy
  65. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  66. Creation and Dissemination of Policies and Related Documentation
  67. Procedure for Dealing with Misconduct in Scholarly Research
  68. Reporting Research Misconduct
  69. Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
  70. Study Closure
  71. Exempt Research (for non-federally funded, non-FDA-regulated, non-VA research)
  72. Research with Adult Participants Lacking Capacity to Consent
  73. De-Identified Publicly Available Datasets Guidance
  74. IRB Composition and Quality Performance
  75. Reporting to Institutional and External Authorities
  76. Review of Data and Safety Monitoring in Research
  77. Maintenance of IRB Records
  78. ED/SBS IRB Principal Investigator Responsibilities
  79. All Campus Animal Care and Advisory Committee Meeting Schedule
  80. PI Status for UW-Madison hESC Protocols
  81. Sub-recipients for PHS Funded Research
  82. Management Plan Notification Letter Example
  83. Contact Information for Reporting Suggestions and Concerns
  84. Good Clinical Practice (GCP) Refresher Instructions
  85. UW HRPP Quality Assurance
  86. UW-Madison Guidance for Investigators Requesting to Add hESC Lines to the UW-Madison hESC Registry
  87. UW-Madison SCRO Initial Review, Continuing Review, and Changes of Protocol Policy
  88. UW-Madison Policy for Full Committee or Expedited Panel Review of Studies Using Human Embryo and or Human Pluripotent Stem Cells
  89. Cross-Campus Human Research Protection Program (HRPP) Committee Charter
  90. Developing an Internal Quality Assurance (QA) Program Guidance
  91. Monitoring the Consent Process
  92. Exceptions to Informed Consent Requirements in Emergency Situations
  93. Considerations for Accepting or Ceding IRB Review Guidance
  94. Suspension and Termination of Approved Research
  95. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  96. Use of Human Fetal Tissue in Research Policy Links
  97. Student Research
  98. IRB Review of Study Resources
  99. List of Approved De-Identified Publicly Available Datasets
  100. Preventing Noncompliance Guidance
  101. IRB Analysis of Risks and Benefits of Research Guidance
  102. NIH Genomic Data Sharing Policy for Human Data Guidance
  103. Conflicts of Interest of Non-UW-Madison Key Personnel
  104. IRB Meeting Minutes and Regulatory Documentation
  105. Unanticipated Problems
  106. Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
  107. IRB Purview
  108. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  109. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  110. Initial Review: Submission and Review Policy
  111. IRB Meetings
  112. Use of Human Fetal Tissue in Research
  113. OHRP Continuing Review Guidance
  114. IRB Authority and Independence
  115. Retention of IRB Records
  116. Compliance Monitoring and Quality Improvement
  117. HRPP and IRB Resources
  118. Campus IT Policies
  119. Human Participants Research
  120. FDA IRB Regulations (21 CFR 56)
  121. HRPP Resources for the Public
  122. Expert Review
  123. Reportable Abuse and Neglect Guidance
  124. OHRP & FDA Expedited Review Guidance
  125. Compliance with Human Research Protections in Sponsored Research
  126. ED/SBS IRB Office Guidance Index
  127. UW-Madison HIPAA Program
  128. IRB Consultants Use and Conflict of Interest
  129. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  130. Common Rule (45 CFR 46)
  131. Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
  132. Quality Assurance Committees
  133. Post Approval Monitoring Program Services
  134. UW Post-Approval Monitors
  135. Bioethics Advisory Commitee on hESC Research
  136. UW-Madison SCRO Multisite Research Policy
  137. UW-Madison Guidance on Research involving the Creation of Human/Nonhuman Chimeras
  138. UW-Madison SCRO Committee Conflict of Interest Policy
  139. Request for Approval to Serve as PI
  140. Mentor and Trainee Responsibilities
  141. Data Acquisition, Management, Sharing and Ownership
  142. Collaborative Research
  143. Animal Research
  144. Conflict of Interest
  145. SCRO Committee: UW-Madison hESC Registry
  146. NIH Training Topics
  147. Institutional Conflict of Interest (ICOI) Procedures
  148. Institutional Conflict of Interest (ICOI) Policy
  149. COI Committee: Evaluating Conflicts of Interest
  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