Results: 1-20 of 68

No.Document TitleIDUpdatedViews
1Recruitment of Research Participants Guidance295602024-10-1817586
2ED/SBS IRB Principal Investigator Responsibilities557692024-10-186390
3Contact Information for Reporting Suggestions and Concerns568892024-10-189654
4Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186904
5Use of Human Fetal Tissue in Research289972024-10-1812599
6Unanticipated Problems295062024-10-1810429
7Suspension and Termination of Approved Research295222024-10-189325
8Study Closure506222024-10-1810404
9Student Research291682024-10-1810077
10Research with Adult Participants Lacking Capacity to Consent295452024-10-1813664
11Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188765
12Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823053
13Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818847
14Noncompliance295072024-10-1819110
15Obtaining and Documenting Informed Consent297622024-10-1813590
16Monitoring the Consent Process295632024-10-187061
17Maintenance of IRB Records294762024-10-187428
18IRB Review of Study Resources291672024-10-186132
19IRB Reliance295652024-10-1811592
20IRB Purview422732024-10-188708

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