Results: 1-20 of 69

No.Document TitleIDUpdatedViews
1Recruitment of Research Participants Guidance295602024-10-1817048
2ED/SBS IRB Principal Investigator Responsibilities557692024-10-185878
3Contact Information for Reporting Suggestions and Concerns568892024-10-189074
4Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186467
5Use of Human Fetal Tissue in Research289972024-10-1811987
6Unanticipated Problems295062024-10-189856
7Suspension and Termination of Approved Research295222024-10-188786
8Study Closure506222024-10-189959
9Student Research291682024-10-189615
10Research with Adult Participants Lacking Capacity to Consent295452024-10-1812618
11Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188273
12Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822512
13Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818231
14Noncompliance295072024-10-1818658
15Obtaining and Documenting Informed Consent297622024-10-1813180
16Monitoring the Consent Process295632024-10-186784
17Maintenance of IRB Records294762024-10-186990
18IRB Review of Study Resources291672024-10-185844
19IRB Reliance295652024-10-1811144
20IRB Purview422732024-10-188324
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