Results: 1–20 of 44

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NumberDocument TitleIDUpdatedViews
1Noncompliance295072024-10-1819380
2Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-189025
3Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823367
4Research with Adult Participants Lacking Capacity to Consent295452024-10-1813978
5Suspension and Termination of Approved Research295222024-10-189587
6Unanticipated Problems295062024-10-1810659
7Use of Human Fetal Tissue in Research289972024-10-1812954
8Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187177
9ED/SBS IRB Principal Investigator Responsibilities557692024-10-186676
10Study Closure506222024-10-1810680
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819211
12Obtaining and Documenting Informed Consent297622024-10-1813886
13Monitoring the Consent Process295632024-10-187300
14Maintenance of IRB Records294762024-10-187684
15IRB Review of Study Resources291672024-10-186358
16IRB Reliance295652024-10-1811866
17IRB Purview422732024-10-188983
18IRB Members’ Conflicts of Interest294662024-10-1811201
19Reporting to Institutional and External Authorities291782024-10-189025
20Initial Review: Submission and Review Policy289372024-10-1810167

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