Results: 41–60 of 125

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NumberDocument TitleIDUpdatedViews
41Reportable Abuse and Neglect Guidance591102017-10-037532
42Clinical Trials Registration & Results Reporting340442024-10-1861594
43Contact Information for Reporting Suggestions and Concerns568892024-10-1810023
44Research Participants341002024-10-188124
45Instructions for Completing CITI Human Participants Research Training325592024-10-18196580
46ED/SBS IRB Principal Investigator Responsibilities557692024-10-186833
47Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187330
48Study Closure506222024-10-1810831
49UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement332802025-10-0226151
50UW Post-Approval Monitors468582024-10-186928
51UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers340482024-10-1816761
52Good Clinical Practice (GCP) Refresher Instructions624332024-10-1813077
53Reporting Research Misconduct344862024-06-0512536
54Misconduct in Scholarly Research344842026-01-2620593
55Responsible Conduct of Research344832018-04-0614145
56Institutional Responsible Conduct of Research (RCR) Plan1502992025-05-06846
57Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy739912020-11-247423
58Compliance with Human Research Protections in Sponsored Research295542020-11-236901
59Institutional Conflict of Interest (ICOI) Procedures585762024-01-038024
60Human Subjects Research Protection Program (HRPP) Policy Index341012020-11-3055406

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