Results: 1-20 of 44

No.Document TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-186141
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186641
3Use of Human Fetal Tissue in Research289972024-10-1812254
4Unanticipated Problems295062024-10-1810227
5Suspension and Termination of Approved Research295222024-10-189155
6Study Closure506222024-10-1810165
7Student Research291682024-10-189840
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1813309
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188548
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822737
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818473
12Noncompliance295072024-10-1818823
13Obtaining and Documenting Informed Consent297622024-10-1813375
14Monitoring the Consent Process295632024-10-186903
15Maintenance of IRB Records294762024-10-187158
16IRB Review of Study Resources291672024-10-185967
17IRB Reliance295652024-10-1811348
18IRB Purview422732024-10-188468
19IRB Members’ Conflicts of Interest294662024-10-1810706
20Reporting to Institutional and External Authorities291782024-10-188483
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