Results: 61–80 of 125

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Search results updated. Showing 20 documents in Table format.
NumberDocument TitleIDUpdatedViews
61IRB Review of Study Resources291672024-10-186416
62Maintenance of IRB Records294762024-10-187733
63Monitoring the Consent Process295632024-10-187343
64Obtaining and Documenting Informed Consent297622024-10-1813944
65Noncompliance295072024-10-1819441
66Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819276
67Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823441
68Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-189087
69Research with Adult Participants Lacking Capacity to Consent295452024-10-1814059
70Student Research291682024-10-1810596
71Suspension and Termination of Approved Research295222024-10-189641
72Unanticipated Problems295062024-10-1810702
73Use of Human Fetal Tissue in Research289972024-10-1813031
74Recruitment of Research Participants Guidance295602024-10-1817878
75Sub-recipients for PHS Funded Research355382024-10-2410994
76Mentor and Trainee Responsibilities333922024-12-028118
77Conflict of Interest Training Course329862024-12-1152405
78Frequently Asked Questions About Time Commitments Reporting1083562025-03-1113576
79Principal Investigator (PI) Status331212025-05-0212145
80The Stem Cell Research Oversight (SCRO) Committee Meeting Dates and Deadlines332832025-05-209635

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