Results: 1–20 of 44

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NumberDocument TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-186547
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187050
3Use of Human Fetal Tissue in Research289972024-10-1812762
4Unanticipated Problems295062024-10-1810541
5Suspension and Termination of Approved Research295222024-10-189473
6Study Closure506222024-10-1810542
7Student Research291682024-10-1810410
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1813834
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188902
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823220
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819046
12Noncompliance295072024-10-1819251
13Obtaining and Documenting Informed Consent297622024-10-1813759
14Monitoring the Consent Process295632024-10-187171
15Maintenance of IRB Records294762024-10-187570
16IRB Review of Study Resources291672024-10-186252
17IRB Reliance295652024-10-1811726
18IRB Purview422732024-10-188853
19IRB Members’ Conflicts of Interest294662024-10-1811091
20Reporting to Institutional and External Authorities291782024-10-188906

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