Results: 1–20 of 44

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NumberDocument TitleIDUpdatedViews
1Noncompliance295072024-10-1819311
2Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188965
3Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823298
4Research with Adult Participants Lacking Capacity to Consent295452024-10-1813895
5Suspension and Termination of Approved Research295222024-10-189530
6Unanticipated Problems295062024-10-1810605
7Use of Human Fetal Tissue in Research289972024-10-1812870
8Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187112
9ED/SBS IRB Principal Investigator Responsibilities557692024-10-186610
10Study Closure506222024-10-1810615
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819128
12Obtaining and Documenting Informed Consent297622024-10-1813819
13Monitoring the Consent Process295632024-10-187249
14Maintenance of IRB Records294762024-10-187627
15IRB Review of Study Resources291672024-10-186309
16IRB Reliance295652024-10-1811791
17IRB Purview422732024-10-188915
18IRB Members’ Conflicts of Interest294662024-10-1811145
19Reporting to Institutional and External Authorities291782024-10-188964
20Initial Review: Submission and Review Policy289372024-10-1810121

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