Results: 1–20 of 44

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NumberDocument TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-186579
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187081
3Use of Human Fetal Tissue in Research289972024-10-1812808
4Unanticipated Problems295062024-10-1810568
5Suspension and Termination of Approved Research295222024-10-189499
6Study Closure506222024-10-1810565
7Student Research291682024-10-1810438
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1813862
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188936
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823259
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819088
12Noncompliance295072024-10-1819276
13Obtaining and Documenting Informed Consent297622024-10-1813791
14Monitoring the Consent Process295632024-10-187204
15Maintenance of IRB Records294762024-10-187594
16IRB Review of Study Resources291672024-10-186275
17IRB Reliance295652024-10-1811754
18IRB Purview422732024-10-188880
19IRB Members’ Conflicts of Interest294662024-10-1811115
20Reporting to Institutional and External Authorities291782024-10-188932

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