Results: 81–100 of 125

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Search results updated. Showing 20 documents in Table format.
NumberDocument TitleIDUpdatedViews
81Good Clinical Practice (GCP) Training Guidance and Instructions611352024-10-1825585
82Instructions for Completing CITI Human Participants Research Training325592024-10-18196046
83Engagement in Human Participants Research at UW–Madison355142024-10-1835451
84Exempt Research291742024-10-1813865
85HRPP and IRB Resources291642024-10-186539
86Initial Review: Submission and Review Policy289372024-10-1810104
87Reporting to Institutional and External Authorities291782024-10-188949
88IRB Members’ Conflicts of Interest294662024-10-1811129
89IRB Purview422732024-10-188895
90IRB Reliance295652024-10-1811769
91IRB Review of Study Resources291672024-10-186293
92Maintenance of IRB Records294762024-10-187610
93Monitoring the Consent Process295632024-10-187222
94Obtaining and Documenting Informed Consent297622024-10-1813804
95Noncompliance295072024-10-1819291
96Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819113
97Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823279
98Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188954
99Research with Adult Participants Lacking Capacity to Consent295452024-10-1813877
100Student Research291682024-10-1810456

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