Results: 121-140 of 168
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No.Document TitleIDUpdatedHits
121 FDA IRB Regulations (21 CFR 56)
544892017-10-031137
122 IRB Meetings
294672017-10-032441
123 Compliance with Human Research Protections in Sponsored Research
295542017-10-031855
124 Exceptions to Informed Consent Requirements in Emergency Situations
295622017-10-031957
125 Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
557992017-10-031429
126 UW-Madison HIPAA Program
557702017-10-031209
127 IRB Consultants Use and Conflict of Interest
294602017-10-032571
128 OHRP Guidance on Engagement of Institutions in Human Subjects Research
497932017-10-031376
129 Common Rule (45 CFR 46)
544882017-10-031272
130 Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
739912017-10-031365
131 HRPP Resources for the Public
341002017-10-033463
132 Expert Review
294512017-10-032987
133 Reportable Abuse and Neglect Guidance
591102017-10-031182
134 Quality Assurance Committees
462622017-09-202010
135 Post Approval Monitoring Program Services
628712017-09-191188
136 UW Post-Approval Monitors
468582017-09-191749
137 Bioethics Advisory Commitee on hESC Research
347192017-09-112498
138 UW-Madison SCRO Multisite Research Policy
347102017-09-111631
139 UW-Madison Guidance on Research involving the Creation of Human/Nonhuman Chimeras
347092017-09-111735
140 UW-Madison SCRO Committee Conflict of Interest Policy
347082017-09-111803

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