Results: 1–20 of 44

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NumberDocument TitleIDUpdatedViews
1Noncompliance295072024-10-1819494
2Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-189164
3Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823522
4Research with Adult Participants Lacking Capacity to Consent295452024-10-1814137
5Suspension and Termination of Approved Research295222024-10-189708
6Unanticipated Problems295062024-10-1810758
7Use of Human Fetal Tissue in Research289972024-10-1813112
8Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187290
9ED/SBS IRB Principal Investigator Responsibilities557692024-10-186789
10Study Closure506222024-10-1810789
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819371
12Obtaining and Documenting Informed Consent297622024-10-1813998
13Monitoring the Consent Process295632024-10-187401
14Maintenance of IRB Records294762024-10-187796
15IRB Review of Study Resources291672024-10-186480
16IRB Reliance295652024-10-1811997
17IRB Purview422732024-10-189112
18IRB Members’ Conflicts of Interest294662024-10-1811347
19Reporting to Institutional and External Authorities291782024-10-189120
20Initial Review: Submission and Review Policy289372024-10-1810271

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