Results: 1–20 of 44

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NumberDocument TitleIDUpdatedViews
1Noncompliance295072024-10-1819521
2Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-189197
3Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823547
4Research with Adult Participants Lacking Capacity to Consent295452024-10-1814171
5Suspension and Termination of Approved Research295222024-10-189733
6Unanticipated Problems295062024-10-1810781
7Use of Human Fetal Tissue in Research289972024-10-1813142
8Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187317
9ED/SBS IRB Principal Investigator Responsibilities557692024-10-186811
10Study Closure506222024-10-1810815
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819402
12Obtaining and Documenting Informed Consent297622024-10-1814023
13Monitoring the Consent Process295632024-10-187427
14Maintenance of IRB Records294762024-10-187817
15IRB Review of Study Resources291672024-10-186497
16IRB Reliance295652024-10-1812016
17IRB Purview422732024-10-189134
18IRB Members’ Conflicts of Interest294662024-10-1811372
19Reporting to Institutional and External Authorities291782024-10-189141
20Initial Review: Submission and Review Policy289372024-10-1810288

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