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