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