1. WISPER Export Control Process FAQ
  2. Export Control Compliance Program
  3. UW-Madison Export Control Program Summary
  4. Principal Investigator (PI) Status
  5. Human Research Protection Program (HRPP) Newsletter - Spring 2017
  6. International Traffic in Arms Regulations (ITAR) FAQs
  7. SCRO Committee: UW-Madison hESC Registry
  8. Conflict of Interest
  9. Collaborative Research
  10. Data Acquisition, Management, Sharing and Ownership
  11. Mentor and Trainee Responsibilities
  12. UW-Madison SCRO Committee Conflict of Interest Policy
  13. UW-Madison SCRO Multisite Research Policy
  14. Bioethics Advisory Commitee on hESC Research
  15. Developing an Internal Quality Assurance (QA) Program Guidance
  16. UW-Madison HIPAA Program
  17. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  18. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  19. Human Participants Research
  20. Preventing Noncompliance Guidance
  21. Considerations for Accepting or Ceding IRB Review Guidance
  22. Campus IT Policies
  23. FDA IRB Regulations (21 CFR 56)
  24. IRB Analysis of Risks and Benefits of Research Guidance
  25. Expert Review
  26. NIH Genomic Data Sharing Policy for Human Data Guidance
  27. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  28. Common Rule (45 CFR 46)
  29. IRB Review of Study Resources
  30. IRB Consultants Use and Conflict of Interest
  31. List of Approved De-Identified Publicly Available Datasets
  32. Reportable Abuse and Neglect Guidance
  33. Use of Human Fetal Tissue in Research Policy Links
  34. Student Research
  35. Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
  36. Conflicts of Interest of Non-UW-Madison Key Personnel
  37. UW-Madison Policy for Full Committee or Expedited Panel Review of Studies Using Human Embryo and or Human Pluripotent Stem Cells
  38. UW-Madison Guidance for Investigators Requesting to Add hESC Lines to the UW-Madison hESC Registry
  39. PI Status for UW-Madison hESC Protocols
  40. ED/SBS IRB Principal Investigator Responsibilities
  41. Maintenance of IRB Records
  42. Review of Data and Safety Monitoring in Research
  43. Reporting to Institutional and External Authorities
  44. De-Identified Publicly Available Datasets Guidance
  45. Reporting Research Misconduct
  46. Procedure for Dealing with Misconduct in Scholarly Research
  47. Creation and Dissemination of Policies and Related Documentation
  48. Research Policy, Compliance, and Safety Training Courses
  49. Office of Research Compliance and Office of Research Policy and Integrity Contacts
  50. Stem Cell Ethics and Policy Training
  51. UW–Madison Policy on Open Research & Free Interchange of Information
  52. Responsible Conduct of Research
  53. Project Assessment Forms
  54. Equitable Selection of Research Participants Guidance
  55. Evaluating the Scientific or Scholarly Merits of Proposed Research
  56. Protecting Research Participants Privacy Interests and Confidentiality of Data
  57. HRPP Newsletter - Spring 2018
  58. IRB Reliance
  59. Request for Approval to Serve as PI
  60. PI Status
  61. Conflict of Interest Training Course
  62. Sub-recipients for PHS Funded Research
  63. Management Plan Notification Letter Example
  64. Reviewer's Tools
  65. USDA NIFA Capacity Fund (142) RCR Training Requirements
  66. Study Closure
  67. Continuing Review: Submission and Review
  68. Retention of IRB Records
  69. Misconduct in Scholarly Research
  70. Obligations and Protections for Graduate Students and Postdoctoral Research Associates in Reporting Wrong Doing, Non-Compliance or Research Misconduct
  71. Issues in Human Subjects Research When State Law May Apply
  72. Export Control Guidance Documents, Templates and Reports
  73. Post-Approval Monitoring Program
  74. COI Committee: Evaluating Conflicts of Interest
  75. Conflict of Interest Policy
  76. Cross-Campus Human Research Protection Program (HRPP) Committee Charter
  77. I-129 Visa Certification Form
  78. Research Participants
  79. Instructions for Completing CITI Human Participants Research Training
  80. Recruitment of Research Participants Guidance
  81. Review of Research Involving Vulnerable Participants
  82. Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
  83. SCRO Protocol Submission
  84. Export Control Training Modules
  85. UW–Madison SCRO Initial Review, Continuing Review, and Changes of Protocol Policy
  86. IRB Members’ Conflicts of Interest
  87. HRPP Education and Training
  88. Suspension and Termination of Approved Research
  89. Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
  90. Unanticipated Problems
  91. Noncompliance
  92. IRB Composition and Quality Performance
  93. IRB Authority and Independence
  94. Institutional Official in Charge of HRPP
  95. HRPP and IRB Resources
  96. Quality Assurance Committees
  97. Exempt Research
  98. Chain of Custody Template
  99. UW HRPP Quality Assurance
  100. UW Post-Approval Monitors
  101. UW–Madison Stem Cell Research Oversight Guidance for Documentation of Provenance
  102. Obtaining and Documenting Informed Consent
  103. Research with Adult Participants Lacking Capacity to Consent
  104. Lab Close-Out Checklist
  105. Compliance Monitoring and Quality Improvement
  106. NIH Training Topics
  107. UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement
  108. Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
  109. Authorship, Publication and Peer Review
  110. Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
  111. Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
  112. Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
  113. Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
  114. UW–Madison United States Department of Agriculture (USDA) National Institute of Food and Agriculture (NIFA) Responsible Conduct of Research (RCR) Training Requirements
  115. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  116. IRB Purview
  117. Initial Review: Submission and Review Policy
  118. UW-Madison Policy for Human Embryo and Human Pluripotent Stem Cell Research
  119. Institutional Conflict of Interest (ICOI) Policy
  120. Institutional Conflict of Interest (ICOI) Procedures
  121. UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
  122. UW-Madison Export Control Organizational Structure
  123. Aircraft Guidance
  124. Guidance for Unammed Aircraft Systems Registration and Insurance
  125. Autonomous Vehicle Guidance
  126. Guidance for Data Management
  127. Individual Financial Conflict of Interest: What to Report
  128. Research Vehicle Safety Oversight (RVSO)
  129. Institutional Conflict of Interest Program
  130. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  131. Contact Information for Reporting Suggestions and Concerns
  132. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  133. IRB Meetings
  134. Exceptions to Informed Consent Requirements in Emergency Situations
  135. Monitoring the Consent Process
  136. Compliance with Human Research Protections in Sponsored Research
  137. Use of Human Fetal Tissue in Research
  138. Academic Staff with Permanent PI Status
  139. Clinical Trials Registration & Results Reporting
  140. Instructions for Linking Previous CITI Training to Your NetID
  141. Unmanned Aircraft System (UAS) Pilot Guidance
  142. The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines
  143. Frequently Asked Questions about Conflict of Interest
  144. Instructions for Completing CITI Refresher Training
  145. Financial Conflict of Interest Management Plan Example
  146. Individual Conflict of Interest: Whom to Contact for Assistance
  147. HRPP Guidance, Forms and Resources
  148. Stem Cell Research Oversight (SCRO) Committee Members
  149. Changes in Research Activities: Submission and Review
  150. IRB Meeting Minutes and Regulatory Documentation
  151. Human Subjects Research Protection Program (HRPP) Policy Index
  152. UW–Madison Office of Research Policy and Integrity Financial Conflict of Interest Policy and Procedures: Guidance Document
  153. Certificate of Confidentiality (CoC) Application Help
  154. All Campus Animal Planning and Advisory Committee Meeting Schedule
  155. Good Clinical Practice (GCP) Refresher Instructions
  156. Human Research Protection Program Newsletter
  157. Human Research Protection Program (HRPP) Newsletter - Fall 2016
  158. Human Research Protection Program (HRPP) Newsletter - Spring 2016
  159. Good Clinical Practice (GCP) Training Guidance and Instructions
  160. UW Human Research Protection Program Newsletter - Fall 2015
  161. Post Approval Monitoring Program Services