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