Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results: 61-80 of 92
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No.Document TitleIDUpdatedHits
61 Maintenance of IRB Records
294762018-02-073423
62 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-072005
63 OHRP Guidance on Engagement of Institutions in Human Subjects Research
497932017-10-032329
64 Expert Review
294512017-10-034184
65 Compliance with Human Research Protections in Sponsored Research
295542017-10-032881
66 Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
507842017-10-032147
67 IRB Review of Study Resources
291672017-10-032858
68 IRB Analysis of Risks and Benefits of Research Guidance
294782017-10-035902
69 Developing an Internal Quality Assurance (QA) Program Guidance
695542017-10-033706
70 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-032478
71 Conflicts of Interest of Non-UW-Madison Key Personnel
297962017-10-033264
72 Monitoring the Consent Process
295632017-10-033356
73 Campus IT Policies
507612017-10-031845
74 Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
739912017-10-032707
75 IRB Consultants Use and Conflict of Interest
294602017-10-033596
76 FDA IRB Regulations (21 CFR 56)
544892017-10-032059
77 Use of Human Fetal Tissue in Research
289972017-10-035337
78 Use of Human Fetal Tissue in Research Policy Links
472182017-10-031873
79 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-031805
80 Preventing Noncompliance Guidance
693702017-10-034336

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