Results: 1-20 of 44

No.Document TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-185841
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186429
3Use of Human Fetal Tissue in Research289972024-10-1811911
4Unanticipated Problems295062024-10-189831
5Suspension and Termination of Approved Research295222024-10-188761
6Study Closure506222024-10-189924
7Student Research291682024-10-189572
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1812545
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188227
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822451
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818188
12Noncompliance295072024-10-1818610
13Obtaining and Documenting Informed Consent297622024-10-1813149
14Monitoring the Consent Process295632024-10-186762
15Maintenance of IRB Records294762024-10-186953
16IRB Review of Study Resources291672024-10-185820
17IRB Reliance295652024-10-1811067
18IRB Purview422732024-10-188281
19IRB Members’ Conflicts of Interest294662024-10-1810373
20Reporting to Institutional and External Authorities291782024-10-187909
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