Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results : 61-80 of 91
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No.Document TitleIDUpdatedHits
61 Study Closure
506222020-11-258368
62 IRB Members’ Conflicts of Interest
294662020-11-248670
63 Use of Human Fetal Tissue in Research
289972020-11-258744
64 Preventing Noncompliance Guidance
693702021-08-098867
65 Compliance Monitoring and Quality Improvement
295472020-11-238972
66 IRB Reliance
295652020-11-249348
67 IRB Analysis of Risks and Benefits of Research Guidance
294782017-10-039408
68 De-Identified Publicly Available Datasets Guidance
294652018-02-079797
69 Continuing Review: Submission and Review
297582020-11-239967
70 Research with Adult Participants Lacking Capacity to Consent
295452020-11-2410168
71 Equitable Selection of Research Participants Guidance
295592018-04-0910920
72 Exempt Research
291742020-11-2311302
73 Obtaining and Documenting Informed Consent
297622020-11-2411377
74 Certificate of Confidentiality (CoC) Application Help
360922022-04-0811487
75 UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
340482022-03-3011933
76 Post-Approval Monitoring Program
462612022-04-1112005
77 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642021-08-0913525
78 Recruitment of Research Participants Guidance
295602021-02-0313864
79 Issues in Human Subjects Research When State Law May Apply
295462022-01-2715431
80 Principal Investigator Status for UW–Madison Studies Involving Human Participants
295572020-11-2415732

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