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