Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
61 Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
548022019-08-054546
62 Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
547972019-08-054540
63 Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
531652019-06-245583
64 UW Post-Approval Monitors
468582019-02-063567
65 UW HRPP Quality Assurance
462602019-02-063515
66 Quality Assurance Committees
462622019-01-223981
67 IRB Authority and Independence
291692019-01-225796
68 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642018-10-0110411
69 Instructions for Completing CITI Human Participants Research Training
325592018-09-25184969
70 Research Participants
341002018-09-175055
71 Issues in Human Subjects Research When State Law May Apply
295462018-08-2812762
72 HRPP Newsletter - Spring 2018
822752018-05-161825
73 Equitable Selection of Research Participants Guidance
295592018-04-099002
74 De-Identified Publicly Available Datasets Guidance
294652018-02-078124
75 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-073006
76 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-033595
77 Use of Human Fetal Tissue in Research Policy Links
472182017-10-032778
78 List of Approved De-Identified Publicly Available Datasets
295502017-10-036605
79 NIH Genomic Data Sharing Policy for Human Data Guidance
495782017-10-034298
80 FDA IRB Regulations (21 CFR 56)
544892017-10-033151

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