Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
61 IRB Consultants Use and Conflict of Interest
294602017-10-032421
62 Unanticipated Problems
295062017-10-033782
63 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-031274
64 Expert Review
294512017-10-032793
65 Monitoring the Consent Process
295632017-10-032087
66 UW-Madison HIPAA Program
557702017-10-031053
67 Campus IT Policies
507612017-10-031023
68 Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
739912017-10-031109
69 HRPP Resources for the Public
341002017-10-033273
70 Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
292312017-10-032202
71 Exceptions to Informed Consent Requirements in Emergency Situations
295622017-10-031851
72 List of Approved De-Identified Publicly Available Datasets
295502017-10-033419
73 Conflicts of Interest of Non-UW-Madison Key Personnel
297962017-10-032059
74 NIH Genomic Data Sharing Policy for Human Data Guidance
495782017-10-031794
75 Initial Review: Submission and Review Policy
289372017-10-033380
76 FDA IRB Regulations (21 CFR 56)
544892017-10-031002
77 IRB Meeting Minutes and Regulatory Documentation
355112017-10-032120
78 Use of Human Fetal Tissue in Research Policy Links
472182017-10-031022
79 Preventing Noncompliance Guidance
693702017-10-031753
80 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-03893

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