Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results: 61-80 of 94
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No.Document TitleIDUpdatedHits
61 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-071843
62 Good Clinical Practice (GCP) Refresher Instructions
624332017-11-173655
63 Monitoring the Consent Process
295632017-10-033128
64 Use of Human Fetal Tissue in Research Policy Links
472182017-10-031713
65 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-031659
66 List of Approved De-Identified Publicly Available Datasets
295502017-10-034673
67 NIH Genomic Data Sharing Policy for Human Data Guidance
495782017-10-032796
68 Conflicts of Interest of Non-UW-Madison Key Personnel
297962017-10-033083
69 FDA IRB Regulations (21 CFR 56)
544892017-10-031863
70 IRB Purview
422732017-10-033840
71 Student Research
291682017-10-034940
72 Reportable Abuse and Neglect Guidance
591102017-10-031951
73 IRB Consultants Use and Conflict of Interest
294602017-10-033409
74 Common Rule (45 CFR 46)
544882017-10-032061
75 Use of Human Fetal Tissue in Research
289972017-10-035056
76 UW-Madison HIPAA Program
557702017-10-031818
77 Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
507842017-10-031998
78 IRB Review of Study Resources
291672017-10-032681
79 Preventing Noncompliance Guidance
693702017-10-033968
80 Developing an Internal Quality Assurance (QA) Program Guidance
695542017-10-033338

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