Results: 101-120 of 168
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No.Document TitleIDUpdatedHits
101 Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
507842017-10-031280
102 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-031011
103 Initial Review: Submission and Review Policy
289372017-10-033657
104 IRB Meetings
294672017-10-032446
105 Use of Human Fetal Tissue in Research
289972017-10-033719
106 OHRP & FDA Expedited Review Guidance
550202017-10-031065
107 IRB Authority and Independence
291692017-10-033057
108 ED/SBS IRB Office Guidance Index
550272017-10-03969
109 HRPP and IRB Resources
291642017-10-032004
110 Campus IT Policies
507612017-10-031162
111 Human Participants Research
333682017-10-031915
112 FDA IRB Regulations (21 CFR 56)
544892017-10-031138
113 HRPP Resources for the Public
341002017-10-033471
114 Expert Review
294512017-10-032991
115 Reportable Abuse and Neglect Guidance
591102017-10-031191
116 Compliance with Human Research Protections in Sponsored Research
295542017-10-031856
117 Exceptions to Informed Consent Requirements in Emergency Situations
295622017-10-031959
118 Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
292312017-10-032418
119 UW-Madison HIPAA Program
557702017-10-031210
120 IRB Consultants Use and Conflict of Interest
294602017-10-032571

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