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 Storage Ransomware Data Protection Features [Campus login required]
  73. Endorsement and Approval of VA Research
  74. Engagement in Human Participants Research at UW–Madison
  75. Equitable Selection of Research Participants Guidance
  76. Exempt Research
  77. FDA Regulated Research Policies and Guidance
  78. Frequently Asked Questions about Collaborative Research Requirements
  79. Genetic Research and Use of Storable Tissues
  80. Globus - Accessing ResearchDrive or SharedDrive Storage with Globus [Campus login required]
  81. Globus - Accessing Restricted ResearchDrive or Secure Shared Drive Storage with Globus [Campus login required]
  82. Globus - Getting Started [Campus login required]
  83. Guidance for Researchers Entering into Outside Consulting Agreements
  84. Guidance for X-Ray Radiation Use in Research Studies for Non-Healing Arts Purposes
  85. Guidance on Exemption: Not Human Subjects Research
  86. Guidance on Research Involving Surveys, Interviews, and Focus Groups
  87. Guidance on Research vs. Quality Improvement and Program Evaluation
  88. Guidance Regarding Drug Shortages and Substitutions that Occur During the Conduct of Research Studies
  89. Guidance Regarding Research that Involves the Collection of Information about Illegal Substance or Alcohol Abuse
  90. Guidance Regarding Self-Experimentation of Researchers as Study Subjects
  91. Guidelines for Genetic Research and the Use of Storable Tissues
  92. HIV Testing in Research Guidance
  93. How does the 5-year expiration date affect my exemption?
  94. HRPP and IRB Resources
  95. HRPP Education and Training
  96. HRPP Guidance, Forms and Resources
  97. HS IRBs News July 2020
  98. HS-IRBs News February 2014
  99. HS-IRBs News January 2012
  100. HS-IRBs News July 2012
  101. HS-IRBs News July 2013
  102. HS-IRBs News June 2013
  103. HS-IRBs News March 2012
  104. HS-IRBs News March 2015
  105. HS-IRBs News May 2012
  106. HS-IRBs News May 2016
  107. HS-IRBs News October 2011
  108. HS-IRBs News October 2013
  109. HS-IRBs News September 2013
  110. HS-IRBs News-December 2011
  111. Human Participants Research
  112. Human Research Protection Program Newsletter
  113. Human Subjects Research [Glossary item]
  114. Human Subjects Research Protection Program (HRPP) Policy Index
  115. I am a student researcher, what IRB approval do I need?
  116. I have samples/images/data that I want to use in a research study. When do I need IRB review?
  117. ICTR OnCore Training Opportunities
  118. IEP Research Community Announcement
  119. Information for Faculty and Staff involved with NIH Training Grants
  120. Initial Review: Submission and Review Policy
  121. Institutional Official in Charge of HRPP
  122. Instructions for Completing CITI Human Participants Research Training
  123. International Agreements
  124. International Research
  125. International Research Guidance
  126. International Traffic in Arms Regulations (ITAR) FAQs
  127. IRB Analysis of Risks and Benefits of Research Guidance
  128. IRB Guidance: Community Based Research Review Practices
  129. IRB Guidance: Deception in Research
  130. IRB Guidance: GDPR and Research at UW
  131. IRB Guidance: International Research
  132. IRB Guidance: Qualitative Research
  133. IRB Guidance: Research and Sponsored Programs (RSP) Release of Grant Funds When Studies Are Ceded to Another Institution's IRB for Review and Approval
  134. IRB Guidance: Research in K-12 Schools
  135. IRB Guidance: Research Involving Prisoners as Participants
  136. IRB Guidance: Research vs. Quality Improvement/Program Evaluation
  137. IRB Guidance: Research with Minors
  138. IRB Guidance: Researchers Leaving UW
  139. IRB Guidance: Technology & New Media Research
  140. IRB Guidance: Use of Student Records in Research
  141. IRB Member Checklist: Research Involving Prisoners as Participants
  142. IRB Purview
  143. IRB QI/Program Evaluation Self-Certification Tool Guidance
  144. IRB Responsibilities Related to Review of VA Research
  145. IRB Review of Study Resources
  146. IRB Workshops & Outreach
  147. Issues in Human Subjects Research When State Law May Apply
  148. Key Personnel Guidance
  149. L&S Academic Services & Support
  150. L&S AOF Resources
  151. L&S Effort Certification Guidance For Certifiers: Commitments, Payroll, Cost Share
  152. L&S Graduate Student Research Opportunities: Graduate Funding Opportunities
  153. L&S Handbook on AOFs
  154. L&S Instructions on Spring 2022 Jobs
  155. L&S Post Degree Training
  156. L&S Pre-Award Services
  157. L&S Pre-Award: Dissertation Improvement Grant Proposals
  158. L&S Pre-Award: Proposal Data & Rates
  159. L&S Pre-Award: Proposal preparation and submission
  160. L&S Pre-Award: Training & Resources
  161. L&S Research Services: Finding Funding
  162. L&S Sabbatical/Research Leave Guidelines
  163. L&S Standard Rates for Short-term Staff and Student Assistants
  164. L&S Student Assistant Appointment Letters
  165. L&S Teaching & Research Professor Titles
  166. L&S Teaching/Research Dual Role Guidelines for Academic Staff
  167. L&S: Progress Reports for NIH Awards (RPPR)
  168. List of Approved De-Identified Publicly Available Datasets
  169. Managing Cisco AMP at the CALS Ag Research Stations
  170. Midwest Area Research Consortium for Health (MARCH) Reliance Fact Sheet
  171. Misconduct in Scholarly Research
  172. NIH STRIDES Program Offerings
  173. Non-English or Limited English Speaking Research Participants Consent Process
  174. Obligations and Protections for Graduate Students and Postdoctoral Research Associates in Reporting Wrong Doing, Non-Compliance or Research Misconduct
  175. Office 365 - Download/Install Office 365
  176. Office 365 - Types of Manifest Groups
  177. Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
  178. Office of Research Compliance and Office of Research Policy and Integrity Contacts
  179. OHRP Guidance on Engagement of Institutions in Human Subjects Research
  180. OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
  181. Overview of IRB Requirements for Multisite and Collaborative Research
  182. Overview of Key Research Concepts under the HIPAA Privacy Rule
  183. Overview of the Accreditation Process and UW-Madison's Human Research Protections Program
  184. PI Status
  185. Policy and Guidance
  186. Post-Approval Monitoring Program
  187. Practical Considerations For The Use Of Immunohistochemistry In Mohs Micrographic Surgery
  188. Principal Investigator (PI) Status
  189. Principal Investigator Status for UW–Madison Studies Involving Human Participants
  190. Procedure for Dealing with Misconduct in Scholarly Research
  191. Procedure for Dealing with Misconduct in Scholarly Research
  192. Protecting Research Participants Privacy Interests and Confidentiality of Data
  193. Protocol Guidance
  194. Public datasets available in cloud providers
  195. Recruitment of Research Participants Guidance
  196. Recruitment of Subjects with Status Relationship with the Research Team
  197. Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
  198. Reporting Research Misconduct
  199. Reporting to Institutional and External Authorities
  200. Research
  201. Research Activities Occurring in an Educational Setting
  202. Research Close-Out Checklist
  203. Research Cyberinfrastructure Cloud Consulting
  204. Research Design and Procedures
  205. Research Participants
  206. Research Policy, Compliance, and Safety Training Courses
  207. Research Vehicle Safety Oversight (RVSO)
  208. Research with Adult Participants Lacking Capacity to Consent
  209. ResearchDrive - Account Modification Form [Campus login required]
  210. ResearchDrive - Admin Guide for Campus IT Staff Supporting Researchers
  211. ResearchDrive - Admin Guide for Campus IT Staff Supporting Researchers With Restricted Data
  212. ResearchDrive - Connecting From a Linux Computer
  213. ResearchDrive - Connecting From a Windows Computer
  214. ResearchDrive - Connecting From an Apple Computer
  215. ResearchDrive - FAQ
  216. ResearchDrive - Getting Started [Campus login required]
  217. ResearchDrive - Requesting Support
  218. ResearchDrive - Restoring Files or Folders from Snapshots
  219. ResearchDrive - Terms of Service [Campus login required]
  220. ResearchDrive - Transferring Data from Box to ResearchDrive
  221. ResearchDrive - Transferring Data with a Linux Computer
  222. ResearchDrive - Transferring Data with a Windows Computer
  223. ResearchDrive - Transferring Data with an Apple Computer
  224. ResearchDrive - Understanding Storage Units GB vs. GiB
  225. ResearchDrive - Working with Collaborators
  226. ResearchDrive - Working With Collaborators If You Have Restricted Data
  227. Responsible Conduct of Research
  228. Retention of IRB Records
  229. REU Stipend Payments to UW Students on NSF and Other Sponsored Funds
  230. Review of Data and Safety Monitoring in Research
  231. Review of FDA-Regulated Research Policy
  232. Review of Research Involving Vulnerable Participants
  233. Robert Draper Technology Innovation Fund (TIF) application documents
  234. Science Research Internship for High School Students
  235. Scientist Screwed Up? Send 'em to Researcher Rehab (2017)
  236. SCRO ARROW Guidance: Getting Started
  237. SCRO ARROW Ongoing Activities Guidance
  238. Should my industry sponsored research study be submitted to a commercial IRB?
  239. State Economic Engagement and Development (SEED) Research Program
  240. Stem Cell Research Oversight (SCRO) Committee Members
  241. Student Assistants [Glossary item]
  242. Student Research
  243. Sub-recipients for PHS Funded Research
  244. Subject Recruitment and Screening Procedures Guidance Index
  245. Suspension and Termination of Approved Research
  246. The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines
  247. Use of Email for Research Purposes Guidance
  248. Use of Human Fetal Tissue in Research
  249. Use of Human Fetal Tissue in Research Policy Links
  250. Using Research Grant Funding for Cloud Services
  251. UW Human Research Protection Program Newsletter - Fall 2015
  252. UW-Madison - IT - Data Classification Policy
  253. UW-Madison - IT - Family Educational Rights and Privacy Act (FERPA)
  254. UW-Madison - IT - Health Insurance Portability and Accountability Act (HIPAA)
  255. UW-Madison - IT - Incident Reporting and Response Policy
  256. UW-Madison - IT - Media and Device Disposal and Reuse Policy
  257. UW-Madison - IT - Non-UW-Madison Applications and Services Guidelines
  258. UW-Madison - IT - Restricted Data Security Management Policy
  259. UW-Madison - IT - Storage and Encryption Policy
  260. UW-Madison Custodian Fund Advances
  261. UW-Madison Policy for Human Embryo and Human Pluripotent Stem Cell Research
  262. UW-Madison Qualtrics - Getting Started
  263. UW-Madison Qualtrics - How to permanently delete a Qualtrics survey you own
  264. UW-Madison Qualtrics - Requirements to transfer surveys to another organization
  265. UW-Madison SCRO Multisite Research Policy
  266. UWMSN - JEMS HIRE - Appointment without PVL/Waiver
  267. UWMSN - JEMS HIRE - Teaching Asst. & Research Asst. Appointments
  268. UW–Madison Intellectual Property Policies and Procedures for University Research
  269. UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement
  270. UW–Madison Office of Research Policy and Integrity Financial Conflict of Interest Policy and Procedures: Guidance Document
  271. UW–Madison Policy on Open Research & Free Interchange of Information
  272. UW–Madison Research Compliance, Protocol, and Safety Related Training Requirements
  273. UW–Madison Stem Cell Research Oversight Guidance for Documentation of Provenance
  274. UW–Madison United States Department of Agriculture (USDA) National Institute of Food and Agriculture (NIFA) Responsible Conduct of Research (RCR) Training Requirements
  275. VA Informed Consent Guidance
  276. VA Research - Overview
  277. VA Research - Policy and Guidance
  278. VA Research: Policy for IRB Review of Human Subjects Research that Falls Under VA Purview
  279. VA Template Documents
  280. Welcome to the Office of the Vice Chancellor for Research and Graduate Education Knowledgebase
  281. What are the criteria to be engaged in human subjects research at UW-Madison?
  282. What do revised U.S. rules mean for human research? (2017)
  283. What documents related to IRB review should be maintained by the study team as part of the research record?
  284. What if I’m planning a new research study that requires face-to-face human subjects research activities?
  285. What if my research involves the use of fetal tissue?
  286. What if researchers have an Initial Review application for a non-COVID-19 study currently under review?
  287. What is required from an IRB standpoint before restarting face-to-face research activities?
  288. What is the IRB review process for COVID-19 research?
  289. 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?
  290. What should I consider before conducting research with vulnerable populations?
  291. What type of application do I need to submit to use samples/images/data for research purposes?
  292. Which State Law(s) should be considered for research?
  293. Who can I contact if I have concerns about human research protections at UW-Madison?