Results: 1-20 of 44

No.Document TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-186207
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186709
3Use of Human Fetal Tissue in Research289972024-10-1812342
4Unanticipated Problems295062024-10-1810265
5Suspension and Termination of Approved Research295222024-10-189186
6Study Closure506222024-10-1810202
7Student Research291682024-10-189892
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1813401
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188604
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822834
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818576
12Noncompliance295072024-10-1818911
13Obtaining and Documenting Informed Consent297622024-10-1813408
14Monitoring the Consent Process295632024-10-186930
15Maintenance of IRB Records294762024-10-187228
16IRB Review of Study Resources291672024-10-186006
17IRB Reliance295652024-10-1811398
18IRB Purview422732024-10-188513
19IRB Members’ Conflicts of Interest294662024-10-1810775
20Reporting to Institutional and External Authorities291782024-10-188555
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