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