1. UW HRPP Quality Assurance
  2. Human Research Protection Program (HRPP) Newsletter - Fall 2016
  3. Human Research Protection Program (HRPP) Newsletter - Spring 2016
  4. Accessing ARROW for Administrative Personnel at UW-Madison Not Engaged in Human Subjects Research
  5. Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
  6. Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
  7. Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
  8. Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
  9. Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
  10. Animal Care and Use Resources
  11. Animal Research
  12. AOF Nomination Form for L&S Departments, 2022-23
  13. Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
  14. Applying for a grant from a cloud provider
  15. Article: "You Don't Know Me, But...": Access to Patient Data and Subject Recruitment in Human Subjects Research
  16. Article: A Comprehensive Analysis of MRI Research Risks: In Support of Full Disclosure
  17. Article: Apple's New ResearchKit: 'Ethics Quagmire' or Medical Research Aid?
  18. Article: As Data Overflows Online, Researchers Grapple With Ethics
  19. Article: Disclosure of Financial Relationships to Participants in Clinical Research
  20. Article: How Variability in the Institutional Review Board Review Process Affects Minimal-Risk Multisite Health Services Research
  21. Article: Lessons from researcher rehab
  22. Article: Pediatric Magnetic Resonance Research and the Minimal-Risk Standard
  23. Article: Updating Research Oversight for the 21st Century
  24. ASA Document 055. Procedures for Dealing with Misconduct in Scholarly Research, 5-15-90
  25. ASA Document 529. Motion Regarding Recommendations on the Organization of Research and Graduate Education
  26. ASA Document 551. Classified Research Report
  27. ASA Document 576. Resolution Regarding Legislative Restrictions on Fetal Tissue Research
  28. ASA Document 639. Endorsement of Policy on Misconduct in Scholarly Research
  29. ASA Document 640. Policy on Misconduct in Scholarly Research
  30. ASA Document 678. Report from Ad Hoc Committee on Research Scientist Titles
  31. ASA Document 681. Resolution Supporting the Recommendation of the Ad Hoc Committee on Research Scientist Titles
  32. ASA Document 706. Resolution Thanking the Faculty Senate for Voting in Favor of Academic Staff Teaching Professor and Research Professor Titles
  33. Autonomous Vehicle Guidance
  34. Big Ten Cancer Research Consortium (BTCRC) Reliance Fact Sheet
  35. Bio-ARROW - Registered Protocols - Create Research Summary for Animal Safety
  36. Bio-ARROW - SmartForm - Research Description
  37. Bioethics Advisory Commitee on hESC Research
  38. Brief Summary of Investigator Responsibilities Related to the Protection of Human Subjects for Exempt Research
  39. Campus Software Library Sigmaplot Installation
  40. Campus Software Library Sigmaplot Troubleshooting
  41. Canvas - Enabled Application Configurations (UW-Madison)
  42. Canvas - Library Dashboard (UW-Madison)
  43. Certificate of Confidentiality (CoC) Application Help
  44. Certify Not Human Subjects Research [Glossary item]
  45. Changes in Research Activities: Submission and Review
  46. Children as research participants: Assent and Consent
  47. Children as research participants: Pregnancy Status
  48. Children as research participants: Regulations
  49. Clinical/Translational Research Proposal
  50. Collaborative Research
  51. Collaborative Research and Single IRB Review
  52. Community Based Research
  53. Completing the Not Research Page
  54. Completing the Research Design and Procedures Section
  55. Compliance Monitoring and Quality Improvement
  56. Compliance with Human Research Protections in Sponsored Research
  57. Conflict of Interest Policy
  58. Conflicts of Interest of Non-UW-Madison Key Personnel
  59. Consent Process for Illiterate Research Participants
  60. Consent Process for Legally Blind Research Participants
  61. Control of Test Articles Used in Research Policy
  62. COVID-19 Related Updates from L&S Administration [Campus login required]
  63. COVID-19 Updates
  64. Cross-Campus Human Research Protection Program (HRPP) Committee Charter
  65. Custom Storage - Terms of Service
  66. Data Digest [Glossary item]
  67. De-Identified Publicly Available Datasets Guidance
  68. Deception in Research Guidance
  69. Do the Safer Badgers building access requirements apply to research participants?
  70. Does my research with coded information or specimens require IRB review?
  71. Does research with existing datasets require IRB review?
  72. DoIT Shared Tools - GitLab for Research
  73. DoIT Storage Ransomware Data Protection Features [Campus login required]
  74. Endorsement and Approval of VA Research
  75. Engagement in Human Participants Research at UW–Madison
  76. Equitable Selection of Research Participants Guidance
  77. Exempt Research
  78. FCOI (Financial Conflict of Interest) [Glossary item]
  79. FDA Regulated Research Policies and Guidance
  80. Frequently Asked Questions about Collaborative Research Requirements
  81. Genetic Research and Use of Storable Tissues
  82. Globus - Accessing ResearchDrive or SharedDrive Storage with Globus [Campus login required]
  83. Globus - Accessing Restricted ResearchDrive or Secure Shared Drive Storage with Globus [Campus login required]
  84. Globus - Getting Started [Campus login required]
  85. Guidance for Researchers Entering into Outside Consulting Agreements
  86. Guidance for X-Ray Radiation Use in Research Studies for Non-Healing Arts Purposes
  87. Guidance on Exemption: Not Human Subjects Research
  88. Guidance on Research Involving Surveys, Interviews, and Focus Groups
  89. Guidance on Research vs. Quality Improvement and Program Evaluation
  90. Guidance Regarding Drug Shortages and Substitutions that Occur During the Conduct of Research Studies
  91. Guidance Regarding Research that Involves the Collection of Information about Illegal Substance or Alcohol Abuse
  92. Guidance Regarding Self-Experimentation of Researchers as Study Subjects
  93. Guidelines for Genetic Research and the Use of Storable Tissues
  94. HIV Testing in Research Guidance
  95. How does the 5-year expiration date affect my exemption?
  96. HRPP and IRB Resources
  97. HRPP Education and Training
  98. HRPP Guidance, Forms and Resources
  99. HS IRBs News July 2020
  100. HS-IRBs News February 2014
  101. HS-IRBs News January 2012
  102. HS-IRBs News July 2012
  103. HS-IRBs News July 2013
  104. HS-IRBs News June 2013
  105. HS-IRBs News March 2012
  106. HS-IRBs News March 2015
  107. HS-IRBs News May 2012
  108. HS-IRBs News May 2016
  109. HS-IRBs News October 2011
  110. HS-IRBs News October 2013
  111. HS-IRBs News September 2013
  112. HS-IRBs News-December 2011
  113. Human Participants Research
  114. Human Research Protection Program Newsletter
  115. Human Subjects Research [Glossary item]
  116. Human Subjects Research Protection Program (HRPP) Policy Index
  117. I am a student researcher, what IRB approval do I need?
  118. I have samples/images/data that I want to use in a research study. When do I need IRB review?
  119. IEP Research Community Announcement
  120. Information for Faculty and Staff involved with NIH Training Grants
  121. Initial Review: Submission and Review Policy
  122. Institutional Official in Charge of HRPP
  123. Institutional Responsibilities [Glossary item]
  124. Instructions for Completing CITI Human Participants Research Training
  125. International Agreements
  126. International Research
  127. International Research Guidance
  128. International Traffic in Arms Regulations (ITAR) FAQs
  129. IRB Analysis of Risks and Benefits of Research Guidance
  130. IRB Guidance: Community Based Research Review Practices
  131. IRB Guidance: Deception in Research
  132. IRB Guidance: GDPR and Research at UW
  133. IRB Guidance: International Research
  134. IRB Guidance: Qualitative Research
  135. IRB Guidance: Research and Sponsored Programs (RSP) Release of Grant Funds When Studies Are Ceded to Another Institution's IRB for Review and Approval
  136. IRB Guidance: Research in K-12 Schools
  137. IRB Guidance: Research Involving Prisoners as Participants
  138. IRB Guidance: Research vs. Quality Improvement/Program Evaluation
  139. IRB Guidance: Research with Minors
  140. IRB Guidance: Researchers Leaving UW
  141. IRB Guidance: Technology & New Media Research
  142. IRB Guidance: Use of Student Records in Research
  143. IRB Member Checklist: Research Involving Prisoners as Participants
  144. IRB Purview
  145. IRB QI/Program Evaluation Self-Certification Tool Guidance
  146. IRB Responsibilities Related to Review of VA Research
  147. IRB Review of Study Resources
  148. IRB Workshops & Outreach
  149. Issues in Human Subjects Research When State Law May Apply
  150. Key Personnel Guidance
  151. L&S Academic Services & Support
  152. L&S AOF Resources
  153. L&S Effort Certification Guidance For Certifiers: Commitments, Payroll, Cost Share
  154. L&S Graduate Student Research Opportunities: Graduate Funding Opportunities
  155. L&S Handbook on AOFs
  156. L&S Post Degree Training
  157. L&S Pre-Award Services
  158. L&S Pre-Award: Dissertation Improvement Grant Proposals
  159. L&S Pre-Award: Proposal Data & Rates
  160. L&S Pre-Award: Proposal preparation and submission
  161. L&S Pre-Award: Training & Resources
  162. L&S Research Services: Finding Funding
  163. L&S Sabbatical/Research Leave Guidelines
  164. L&S Standard Rates for Short-term Staff and Student Assistants
  165. L&S Student Assistant Appointment Letters
  166. L&S Teaching & Research Professor Titles
  167. L&S Teaching/Research Dual Role Guidelines for Academic Staff
  168. L&S: Progress Reports for NIH Awards (RPPR)
  169. List of Approved De-Identified Publicly Available Datasets
  170. Managing Cisco AMP at the CALS Ag Research Stations
  171. Midwest Area Research Consortium for Health (MARCH) Reliance Fact Sheet
  172. Misconduct in Scholarly Research
  173. NIH STRIDES Program Offerings
  174. NIH Training Topics
  175. Non-English or Limited English Speaking Research Participants Consent Process
  176. Obligations and Protections for Graduate Students and Postdoctoral Research Associates in Reporting Wrong Doing, Non-Compliance or Research Misconduct
  177. Office 365 - Download/Install Office 365
  178. Office 365 - Types of Manifest Groups
  179. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  180. Office of Research Compliance and Office of Research Policy and Integrity Contacts
  181. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  182. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  183. Overview of IRB Requirements for Multisite and Collaborative Research
  184. Overview of Key Research Concepts under the HIPAA Privacy Rule
  185. Overview of the Accreditation Process and UW-Madison's Human Research Protections Program
  186. PI Status
  187. Policy and Guidance
  188. Post-Approval Monitoring Program
  189. Practical Considerations For The Use Of Immunohistochemistry In Mohs Micrographic Surgery
  190. Principal Investigator (PI) Status
  191. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  192. Procedure for Dealing with Misconduct in Scholarly Research
  193. Procedure for Dealing with Misconduct in Scholarly Research
  194. Protecting Research Participants Privacy Interests and Confidentiality of Data
  195. Protocol Guidance
  196. Public datasets available in cloud providers
  197. Recruitment of Research Participants Guidance
  198. Recruitment of Subjects with Status Relationship with the Research Team
  199. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  200. Reporting Research Misconduct
  201. Reporting to Institutional and External Authorities
  202. Research
  203. Research Activities Occurring in an Educational Setting
  204. Research Close-Out Checklist
  205. Research Cyberinfrastructure Cloud Consulting
  206. Research Design and Procedures
  207. Research Participants
  208. Research Policy, Compliance, and Safety Training Courses
  209. Research Vehicle Safety Oversight (RVSO)
  210. Research with Adult Participants Lacking Capacity to Consent
  211. ResearchDrive - Account Modification Form [Campus login required]
  212. ResearchDrive - Admin Guide for Campus IT Staff Supporting Researchers
  213. ResearchDrive - Admin Guide for Campus IT Staff Supporting Researchers With Restricted Data
  214. ResearchDrive - Connecting From a Linux Computer
  215. ResearchDrive - Connecting From a Windows Computer
  216. ResearchDrive - Connecting From an Apple Computer
  217. ResearchDrive - FAQ
  218. ResearchDrive - Getting Started [Campus login required]
  219. ResearchDrive - Requesting Support
  220. ResearchDrive - Restoring Files or Folders from Snapshots
  221. ResearchDrive - Terms of Service [Campus login required]
  222. ResearchDrive - Transferring Data from Box to ResearchDrive
  223. ResearchDrive - Transferring Data with a Linux Computer
  224. ResearchDrive - Transferring Data with a Windows Computer
  225. ResearchDrive - Transferring Data with an Apple Computer
  226. ResearchDrive - Understanding Storage Units GB vs. GiB
  227. ResearchDrive - Working with Collaborators
  228. ResearchDrive - Working With Collaborators If You Have Restricted Data
  229. Responsible Conduct of Research
  230. Retention of IRB Records
  231. REU Stipend Payments to UW Students on NSF and Other Sponsored Funds
  232. Review of Data and Safety Monitoring in Research
  233. Review of FDA-Regulated Research Policy
  234. Review of Research Involving Vulnerable Participants
  235. Robert Draper Technology Innovation Fund (TIF) application documents
  236. Science Research Internship for High School Students
  237. Scientist Screwed Up? Send 'em to Researcher Rehab (2017)
  238. SCRO ARROW Guidance: Getting Started
  239. SCRO ARROW Ongoing Activities Guidance
  240. Should my industry sponsored research study be submitted to a commercial IRB?
  241. State Economic Engagement and Development (SEED) Research Program
  242. Stem Cell Research Oversight (SCRO) Committee Members
  243. Student Assistants [Glossary item]
  244. Student Research
  245. Sub-recipient [Glossary item]
  246. Sub-recipients for PHS Funded Research
  247. Subject Recruitment and Screening Procedures Guidance Index
  248. Suspension and Termination of Approved Research
  249. The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines
  250. Use of Email for Research Purposes Guidance
  251. Use of Human Fetal Tissue in Research
  252. Use of Human Fetal Tissue in Research Policy Links
  253. Using Research Grant Funding for Cloud Services
  254. UW Human Research Protection Program Newsletter - Fall 2015
  255. UW-Madison - IT - Data Classification Policy
  256. UW-Madison - IT - Family Educational Rights and Privacy Act (FERPA)
  257. UW-Madison - IT - Health Insurance Portability and Accountability Act (HIPAA)
  258. UW-Madison - IT - Incident Reporting and Response Policy
  259. UW-Madison - IT - Media and Device Disposal and Reuse Policy
  260. UW-Madison - IT - Non-UW-Madison Applications and Services Guidelines
  261. UW-Madison - IT - Restricted Data Security Management Policy
  262. UW-Madison - IT - Storage and Encryption Policy
  263. UW-Madison Custodian Fund Advances
  264. UW-Madison Policy for Human Embryo and Human Pluripotent Stem Cell Research
  265. UW-Madison Qualtrics - Getting Started
  266. UW-Madison Qualtrics - How to permanently delete a Qualtrics survey you own
  267. UW-Madison Qualtrics - Requirements to transfer surveys to another organization
  268. UW-Madison SCRO Multisite Research Policy
  269. UWMSN - JEMS HIRE - Appointment without PVL/Waiver
  270. UWMSN - JEMS HIRE - Teaching Asst. & Research Asst. Appointments
  271. UW–Madison Intellectual Property Policies and Procedures for University Research
  272. UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement
  273. UW–Madison Office of Research Policy and Integrity Financial Conflict of Interest Policy and Procedures: Guidance Document
  274. UW–Madison Policy on Open Research & Free Interchange of Information
  275. UW–Madison Research Compliance, Protocol, and Safety Related Training Requirements
  276. UW–Madison Stem Cell Research Oversight Guidance for Documentation of Provenance
  277. UW–Madison United States Department of Agriculture (USDA) National Institute of Food and Agriculture (NIFA) Responsible Conduct of Research (RCR) Training Requirements
  278. VA Informed Consent Guidance
  279. VA Research - Overview
  280. VA Research - Policy and Guidance
  281. VA Research: Policy for IRB Review of Human Subjects Research that Falls Under VA Purview
  282. VA Template Documents
  283. Welcome to the Office of the Vice Chancellor for Research and Graduate Education Knowledgebase
  284. What are the criteria to be engaged in human subjects research at UW-Madison?
  285. What do revised U.S. rules mean for human research? (2017)
  286. What documents related to IRB review should be maintained by the study team as part of the research record?
  287. What if I’m planning a new research study that requires face-to-face human subjects research activities?
  288. What if my research involves the use of fetal tissue?
  289. What if researchers have an Initial Review application for a non-COVID-19 study currently under review?
  290. What is required from an IRB standpoint before restarting face-to-face research activities?
  291. What is the IRB review process for COVID-19 research?
  292. What role can the IRB play for department chairs, center directors, and deans who are determining whether specific research studies can reopen face-to-face visits?
  293. What should I consider before conducting research with vulnerable populations?
  294. What type of application do I need to submit to use samples/images/data for research purposes?
  295. Which State Law(s) should be considered for research?