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