Results: 1-20 of 68

No.Document TitleIDUpdatedViews
1Recruitment of Research Participants Guidance295602024-10-1817570
2ED/SBS IRB Principal Investigator Responsibilities557692024-10-186366
3Contact Information for Reporting Suggestions and Concerns568892024-10-189630
4Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186888
5Use of Human Fetal Tissue in Research289972024-10-1812587
6Unanticipated Problems295062024-10-1810418
7Suspension and Termination of Approved Research295222024-10-189311
8Study Closure506222024-10-1810389
9Student Research291682024-10-1810066
10Research with Adult Participants Lacking Capacity to Consent295452024-10-1813641
11Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188752
12Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823035
13Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818822
14Noncompliance295072024-10-1819100
15Obtaining and Documenting Informed Consent297622024-10-1813578
16Monitoring the Consent Process295632024-10-187053
17Maintenance of IRB Records294762024-10-187411
18IRB Review of Study Resources291672024-10-186117
19IRB Reliance295652024-10-1811579
20IRB Purview422732024-10-188690

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