Results: 1-20 of 44

No.Document TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-186450
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186947
3Use of Human Fetal Tissue in Research289972024-10-1812660
4Unanticipated Problems295062024-10-1810460
5Suspension and Termination of Approved Research295222024-10-189385
6Study Closure506222024-10-1810458
7Student Research291682024-10-1810120
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1813729
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188811
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823123
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818929
12Noncompliance295072024-10-1819162
13Obtaining and Documenting Informed Consent297622024-10-1813659
14Monitoring the Consent Process295632024-10-187098
15Maintenance of IRB Records294762024-10-187481
16IRB Review of Study Resources291672024-10-186176
17IRB Reliance295652024-10-1811650
18IRB Purview422732024-10-188760
19IRB Members’ Conflicts of Interest294662024-10-1811011
20Reporting to Institutional and External Authorities291782024-10-188827

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