Results: 81-100 of 168
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No.Document TitleIDUpdatedHits
81 Compliance Monitoring and Quality Improvement
295472017-10-033690
82 NIH Genomic Data Sharing Policy for Human Data Guidance
495782017-10-031567
83 IRB Meeting Minutes and Regulatory Documentation
355112017-10-031892
84 HRPP and IRB Resources
291642017-10-031646
85 Campus IT Policies
507612017-10-03841
86 FDA IRB Regulations (21 CFR 56)
544892017-10-03828
87 Review of Research Involving Vulnerable Participants
297612017-10-035586
88 Institutional Officials in Charge of HRPP
291632017-10-032817
89 Recruitment of Research Participants Guidance
295602017-10-035499
90 Human Subjects Research Protection Program (HRPP) Policy Index
341012017-10-0332547
91 Retention of IRB Records
294772017-10-033092
92 Reportable Abuse and Neglect Guidance
591102017-10-03840
93 IRB Consultants Use and Conflict of Interest
294602017-10-032187
94 Use of Human Fetal Tissue in Research
289972017-10-033175
95 Creation and Dissemination of Policies and Related Documentation
297562017-10-032255
96 IRB Authority and Independence
291692017-10-032614
97 UW-Madison HIPAA Program
557702017-10-03812
98 OHRP Guidance on Engagement of Institutions in Human Subjects Research
497932017-10-031002
99 IRB Analysis of Risks and Benefits of Research Guidance
294782017-10-033162
100 Common Rule (45 CFR 46)
544882017-10-03906

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