Results: 1-20 of 44

No.Document TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-185879
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186468
3Use of Human Fetal Tissue in Research289972024-10-1811992
4Unanticipated Problems295062024-10-189857
5Suspension and Termination of Approved Research295222024-10-188786
6Study Closure506222024-10-189959
7Student Research291682024-10-189616
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1812620
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188273
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822512
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818231
12Noncompliance295072024-10-1818658
13Obtaining and Documenting Informed Consent297622024-10-1813181
14Monitoring the Consent Process295632024-10-186786
15Maintenance of IRB Records294762024-10-186993
16IRB Review of Study Resources291672024-10-185844
17IRB Reliance295652024-10-1811146
18IRB Purview422732024-10-188326
19IRB Members’ Conflicts of Interest294662024-10-1810478
20Reporting to Institutional and External Authorities291782024-10-187936
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