1. Instructions for Completing CITI Human Participants Research Training
  2. Instructions for Linking Previous CITI Training to Your NetID
  3. Clinical Trials Registration & Results Reporting
  4. Human Subjects Research Protection Program (HRPP) Policy Index
  5. Engagement in Human Participants Research at UW–Madison
  6. Instructions for Completing CITI Refresher Training
  7. Review of Research Involving Vulnerable Participants
  8. Protecting Research Participants Privacy Interests and Confidentiality of Data
  9. HRPP Guidance, Forms and Resources
  10. Good Clinical Practice (GCP) Training Guidance and Instructions
  11. Noncompliance
  12. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  13. Issues in Human Subjects Research When State Law May Apply
  14. Recruitment of Research Participants Guidance
  15. Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
  16. Obtaining and Documenting Informed Consent
  17. Post-Approval Monitoring Program
  18. Certificate of Confidentiality (CoC) Application Help
  19. UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
  20. Exempt Research
  21. Equitable Selection of Research Participants Guidance
  22. Continuing Review: Submission and Review
  23. Research with Adult Participants Lacking Capacity to Consent
  24. De-Identified Publicly Available Datasets Guidance
  25. IRB Reliance
  26. IRB Analysis of Risks and Benefits of Research Guidance
  27. Compliance Monitoring and Quality Improvement
  28. IRB Members’ Conflicts of Interest
  29. Use of Human Fetal Tissue in Research
  30. Unanticipated Problems
  31. Study Closure
  32. Student Research
  33. Preventing Noncompliance Guidance
  34. Initial Review: Submission and Review Policy
  35. List of Approved De-Identified Publicly Available Datasets
  36. Good Clinical Practice (GCP) Refresher Instructions
  37. Retention of IRB Records
  38. HRPP Education and Training
  39. Suspension and Termination of Approved Research
  40. Changes in Research Activities: Submission and Review
  41. Developing an Internal Quality Assurance (QA) Program Guidance
  42. IRB Authority and Independence
  43. Institutional Official in Charge of HRPP
  44. IRB Purview
  45. Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
  46. Cross-Campus Human Research Protection Program (HRPP) Committee Charter
  47. Contact Information for Reporting Suggestions and Concerns
  48. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  49. Reporting to Institutional and External Authorities
  50. IRB Composition and Quality Performance
  51. Research Participants
  52. Creation and Dissemination of Policies and Related Documentation
  53. Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
  54. Review of Data and Safety Monitoring in Research
  55. Maintenance of IRB Records
  56. Monitoring the Consent Process
  57. IRB Consultants Use and Conflict of Interest
  58. IRB Meetings
  59. IRB Meeting Minutes and Regulatory Documentation
  60. Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
  61. Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
  62. Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
  63. NIH Genomic Data Sharing Policy for Human Data Guidance
  64. Conflicts of Interest of Non-UW-Madison Key Personnel
  65. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  66. Compliance with Human Research Protections in Sponsored Research
  67. Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
  68. HRPP and IRB Resources
  69. Quality Assurance Committees
  70. Exceptions to Informed Consent Requirements in Emergency Situations
  71. IRB Review of Study Resources
  72. Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
  73. Considerations for Accepting or Ceding IRB Review Guidance
  74. Human Research Protection Program Newsletter
  75. UW Post-Approval Monitors
  76. UW HRPP Quality Assurance
  77. Common Rule (45 CFR 46)
  78. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  79. Reportable Abuse and Neglect Guidance
  80. FDA IRB Regulations (21 CFR 56)
  81. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  82. ED/SBS IRB Principal Investigator Responsibilities
  83. Human Research Protection Program (HRPP) Newsletter - Fall 2016
  84. UW-Madison HIPAA Program
  85. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  86. Human Research Protection Program (HRPP) Newsletter - Spring 2016
  87. Post Approval Monitoring Program Services
  88. Use of Human Fetal Tissue in Research Policy Links
  89. UW Human Research Protection Program Newsletter - Fall 2015
  90. Campus IT Policies
  91. HRPP Newsletter - Spring 2018