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. Human Participants Research
  21. Developing an Internal Quality Assurance (QA) Program Guidance
  22. UW-Madison HIPAA Program
  23. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  24. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  25. Preventing Noncompliance Guidance
  26. Considerations for Accepting or Ceding IRB Review Guidance
  27. Campus IT Policies
  28. FDA IRB Regulations (21 CFR 56)
  29. IRB Analysis of Risks and Benefits of Research Guidance
  30. IRB Consultants Use and Conflict of Interest
  31. List of Approved De-Identified Publicly Available Datasets
  32. Expert Review
  33. NIH Genomic Data Sharing Policy for Human Data Guidance
  34. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  35. Common Rule (45 CFR 46)
  36. IRB Review of Study Resources
  37. Reportable Abuse and Neglect Guidance
  38. Use of Human Fetal Tissue in Research Policy Links
  39. Student Research
  40. Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
  41. Conflicts of Interest of Non-UW-Madison Key Personnel
  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. USDA NIFA Capacity Fund (142) RCR Training Requirements
  73. Study Closure
  74. Continuing Review: Submission and Review
  75. Retention of IRB Records
  76. Misconduct in Scholarly Research
  77. Obligations and Protections for Graduate Students and Postdoctoral Research Associates in Reporting Wrong Doing, Non-Compliance or Research Misconduct
  78. Issues in Human Subjects Research When State Law May Apply
  79. Export Control Guidance Documents, Templates and Reports
  80. Post-Approval Monitoring Program
  81. COI Committee: Evaluating Conflicts of Interest
  82. Conflict of Interest Policy
  83. Cross-Campus Human Research Protection Program (HRPP) Committee Charter
  84. I-129 Visa Certification Form
  85. Research Participants
  86. Instructions for Completing CITI Human Participants Research Training
  87. Recruitment of Research Participants Guidance
  88. Review of Research Involving Vulnerable Participants
  89. Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
  90. SCRO Protocol Submission
  91. Export Control Training Modules
  92. UW–Madison SCRO Initial Review, Continuing Review, and Changes of Protocol Policy
  93. IRB Members’ Conflicts of Interest
  94. IRB Meeting Minutes and Regulatory Documentation
  95. HRPP Education and Training
  96. Suspension and Termination of Approved Research
  97. Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
  98. Unanticipated Problems
  99. Noncompliance
  100. IRB Composition and Quality Performance
  101. IRB Authority and Independence
  102. Institutional Official in Charge of HRPP
  103. HRPP and IRB Resources
  104. Quality Assurance Committees
  105. Exempt Research
  106. Chain of Custody Template
  107. UW HRPP Quality Assurance
  108. UW Post-Approval Monitors
  109. UW–Madison Stem Cell Research Oversight Guidance for Documentation of Provenance
  110. Obtaining and Documenting Informed Consent
  111. Research with Adult Participants Lacking Capacity to Consent
  112. Lab Close-Out Checklist
  113. Compliance Monitoring and Quality Improvement
  114. NIH Training Topics
  115. UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement
  116. Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
  117. Authorship, Publication and Peer Review
  118. Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
  119. Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
  120. Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
  121. Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
  122. UW–Madison United States Department of Agriculture (USDA) National Institute of Food and Agriculture (NIFA) Responsible Conduct of Research (RCR) Training Requirements
  123. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  124. IRB Purview
  125. Initial Review: Submission and Review Policy
  126. Stem Cell Research Oversight (SCRO) Committee Members
  127. Good Clinical Practice (GCP) Refresher Instructions
  128. UW-Madison Policy for Human Embryo and Human Pluripotent Stem Cell Research
  129. Institutional Conflict of Interest (ICOI) Policy
  130. Institutional Conflict of Interest (ICOI) Procedures
  131. HRPP Guidance, Forms and Resources
  132. Engagement in Human Participants Research at UW–Madison
  133. UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
  134. UW-Madison Export Control Organizational Structure
  135. Good Clinical Practice (GCP) Training Guidance and Instructions
  136. Aircraft Guidance
  137. Guidance for Unammed Aircraft Systems Registration and Insurance
  138. Autonomous Vehicle Guidance
  139. Guidance for Data Management
  140. Individual Financial Conflict of Interest: What to Report
  141. UW–Madison Office of Research Policy and Integrity Financial Conflict of Interest Policy and Procedures: Guidance Document
  142. Research Vehicle Safety Oversight (RVSO)
  143. Institutional Conflict of Interest Program
  144. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  145. Contact Information for Reporting Suggestions and Concerns
  146. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  147. IRB Meetings
  148. Exceptions to Informed Consent Requirements in Emergency Situations
  149. Monitoring the Consent Process
  150. Compliance with Human Research Protections in Sponsored Research
  151. Use of Human Fetal Tissue in Research
  152. Human Subjects Research Protection Program (HRPP) Policy Index
  153. Academic Staff with Permanent PI Status
  154. Clinical Trials Registration & Results Reporting
  155. All Campus Animal Planning and Advisory Committee Meeting Schedule
  156. Certificate of Confidentiality (CoC) Application Help
  157. Instructions for Linking Previous CITI Training to Your NetID
  158. Unmanned Aircraft System (UAS) Pilot Guidance
  159. The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines
  160. Individual Conflict of Interest: Whom to Contact for Assistance
  161. Frequently Asked Questions about Conflict of Interest
  162. Instructions for Completing CITI Refresher Training