Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results : 61-80 of 90
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No.Document TitleIDUpdatedHits
61 Human Research Protection Program Newsletter
565352020-04-024692
62 Good Clinical Practice (GCP) Refresher Instructions
624332020-04-028693
63 Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
555332019-08-196098
64 Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
555892019-08-056251
65 Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
548022019-08-056655
66 Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
547972019-08-056595
67 Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
531652019-06-247696
68 UW Post-Approval Monitors
468582019-02-064800
69 UW HRPP Quality Assurance
462602019-02-064675
70 Quality Assurance Committees
462622019-01-225262
71 IRB Authority and Independence
291692019-01-227055
72 Instructions for Completing CITI Human Participants Research Training
325592018-09-25189196
73 Research Participants
341002018-09-176105
74 Equitable Selection of Research Participants Guidance
295592018-04-0911418
75 De-Identified Publicly Available Datasets Guidance
294652018-02-0710202
76 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-074369
77 Common Rule (45 CFR 46)
544882017-10-034779
78 IRB Consultants Use and Conflict of Interest
294602017-10-035741
79 FDA IRB Regulations (21 CFR 56)
544892017-10-034265
80 IRB Analysis of Risks and Benefits of Research Guidance
294782017-10-039789

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