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Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
1 Common Rule (45 CFR 46)
544882017-10-034898
2 IRB Consultants Use and Conflict of Interest
294602017-10-035822
3 FDA IRB Regulations (21 CFR 56)
544892017-10-034365
4 UW-Madison HIPAA Program
557702017-10-034162
5 IRB Analysis of Risks and Benefits of Research Guidance
294782017-10-039990
6 Use of Human Fetal Tissue in Research Policy Links
472182017-10-034020
7 List of Approved De-Identified Publicly Available Datasets
295502017-10-038923
8 Campus IT Policies
507612017-10-033668
9 Reportable Abuse and Neglect Guidance
591102017-10-034861
10 Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
507842017-10-034243
11 NIH Genomic Data Sharing Policy for Human Data Guidance
495782017-10-035793
12 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-035184
13 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-034119
14 OHRP Guidance on Engagement of Institutions in Human Subjects Research
497932017-10-034778
15 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-074523
16 De-Identified Publicly Available Datasets Guidance
294652018-02-0710407
17 Equitable Selection of Research Participants Guidance
295592018-04-0911706
18 Research Participants
341002018-09-176209
19 Instructions for Completing CITI Human Participants Research Training
325592018-09-25189525
20 IRB Authority and Independence
291692019-01-227172

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