Results: 1-20 of 44

No.Document TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-185931
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186512
3Use of Human Fetal Tissue in Research289972024-10-1812071
4Unanticipated Problems295062024-10-189896
5Suspension and Termination of Approved Research295222024-10-188854
6Study Closure506222024-10-1810014
7Student Research291682024-10-189648
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1812664
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188340
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822575
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818293
12Noncompliance295072024-10-1818707
13Obtaining and Documenting Informed Consent297622024-10-1813233
14Monitoring the Consent Process295632024-10-186824
15Maintenance of IRB Records294762024-10-187038
16IRB Review of Study Resources291672024-10-185882
17IRB Reliance295652024-10-1811203
18IRB Purview422732024-10-188356
19IRB Members’ Conflicts of Interest294662024-10-1810556
20Reporting to Institutional and External Authorities291782024-10-187996
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