Results: 1–20 of 44

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NumberDocument TitleIDUpdatedViews
1Noncompliance295072024-10-1819441
2Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-189087
3Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823441
4Research with Adult Participants Lacking Capacity to Consent295452024-10-1814060
5Suspension and Termination of Approved Research295222024-10-189641
6Unanticipated Problems295062024-10-1810703
7Use of Human Fetal Tissue in Research289972024-10-1813031
8Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187246
9ED/SBS IRB Principal Investigator Responsibilities557692024-10-186728
10Study Closure506222024-10-1810732
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819276
12Obtaining and Documenting Informed Consent297622024-10-1813945
13Monitoring the Consent Process295632024-10-187343
14Maintenance of IRB Records294762024-10-187733
15IRB Review of Study Resources291672024-10-186416
16IRB Reliance295652024-10-1811931
17IRB Purview422732024-10-189044
18IRB Members’ Conflicts of Interest294662024-10-1811285
19Reporting to Institutional and External Authorities291782024-10-189068
20Initial Review: Submission and Review Policy289372024-10-1810218

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