Results: 41–60 of 125

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NumberDocument TitleIDUpdatedViews
41Reportable Abuse and Neglect Guidance591102017-10-037343
42Clinical Trials Registration & Results Reporting340442024-10-1861369
43Contact Information for Reporting Suggestions and Concerns568892024-10-189892
44Research Participants341002024-10-187989
45Instructions for Completing CITI Human Participants Research Training325592024-10-18196240
46ED/SBS IRB Principal Investigator Responsibilities557692024-10-186671
47Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187176
48Study Closure506222024-10-1810678
49UW–Madison National Science Foundation (NSF) Responsible Conduct of Research (RCR) Training Requirement332802025-10-0225960
50UW Post-Approval Monitors468582024-10-186810
51UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers340482024-10-1816620
52Good Clinical Practice (GCP) Refresher Instructions624332024-10-1812886
53Reporting Research Misconduct344862024-06-0512113
54Misconduct in Scholarly Research344842026-01-2620220
55Responsible Conduct of Research344832018-04-0613853
56Institutional Responsible Conduct of Research (RCR) Plan1502992025-05-06690
57Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy739912020-11-247318
58Compliance with Human Research Protections in Sponsored Research295542020-11-236768
59Institutional Conflict of Interest (ICOI) Procedures585762024-01-037773
60Human Subjects Research Protection Program (HRPP) Policy Index341012020-11-3055179

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