Results: 1–20 of 44

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NumberDocument TitleIDUpdatedViews
1Noncompliance295072024-10-1819318
2Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188976
3Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823304
4Research with Adult Participants Lacking Capacity to Consent295452024-10-1813904
5Suspension and Termination of Approved Research295222024-10-189540
6Unanticipated Problems295062024-10-1810613
7Use of Human Fetal Tissue in Research289972024-10-1812876
8Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187119
9ED/SBS IRB Principal Investigator Responsibilities557692024-10-186616
10Study Closure506222024-10-1810627
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819142
12Obtaining and Documenting Informed Consent297622024-10-1813828
13Monitoring the Consent Process295632024-10-187260
14Maintenance of IRB Records294762024-10-187632
15IRB Review of Study Resources291672024-10-186314
16IRB Reliance295652024-10-1811798
17IRB Purview422732024-10-188923
18IRB Members’ Conflicts of Interest294662024-10-1811154
19Reporting to Institutional and External Authorities291782024-10-188968
20Initial Review: Submission and Review Policy289372024-10-1810127

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