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?