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