Results: 21-40 of 125

No.Document TitleIDUpdatedViews
21Use of Human Fetal Tissue in Research289972024-10-1812619
22Unanticipated Problems295062024-10-1810439
23Suspension and Termination of Approved Research295222024-10-189341
24Study Closure506222024-10-1810425
25Student Research291682024-10-1810094
26Research with Adult Participants Lacking Capacity to Consent295452024-10-1813687
27Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188779
28Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823075
29Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818882
30Noncompliance295072024-10-1819123
31Obtaining and Documenting Informed Consent297622024-10-1813613
32Monitoring the Consent Process295632024-10-187072
33Maintenance of IRB Records294762024-10-187448
34IRB Review of Study Resources291672024-10-186145
35IRB Reliance295652024-10-1811614
36IRB Purview422732024-10-188731
37IRB Members’ Conflicts of Interest294662024-10-1810985
38Reporting to Institutional and External Authorities291782024-10-188794
39Initial Review: Submission and Review Policy289372024-10-189992
40HRPP and IRB Resources291642024-10-186424

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