Results: 1-20 of 44

No.Document TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-186271
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186787
3Use of Human Fetal Tissue in Research289972024-10-1812416
4Unanticipated Problems295062024-10-1810316
5Suspension and Termination of Approved Research295222024-10-189235
6Study Closure506222024-10-1810269
7Student Research291682024-10-189968
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1813485
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188666
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822914
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818657
12Noncompliance295072024-10-1818978
13Obtaining and Documenting Informed Consent297622024-10-1813481
14Monitoring the Consent Process295632024-10-186977
15Maintenance of IRB Records294762024-10-187304
16IRB Review of Study Resources291672024-10-186045
17IRB Reliance295652024-10-1811461
18IRB Purview422732024-10-188578
19IRB Members’ Conflicts of Interest294662024-10-1810849
20Reporting to Institutional and External Authorities291782024-10-188654

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