Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results: 21-40 of 92
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No.Document TitleIDUpdatedHits
21 Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
555332019-08-192902
22 Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
548022019-08-053172
23 Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
547972019-08-053082
24 FDA IRB Regulations (21 CFR 56)
544892017-10-032128
25 Common Rule (45 CFR 46)
544882017-10-032315
26 Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
531652019-06-244026
27 Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
507842017-10-032208
28 Campus IT Policies
507612017-10-031886
29 Study Closure
506222018-08-155048
30 OHRP Guidance on Engagement of Institutions in Human Subjects Research
497932017-10-032400
31 NIH Genomic Data Sharing Policy for Human Data Guidance
495782017-10-033148
32 Use of Human Fetal Tissue in Research Policy Links
472182017-10-031921
33 UW Post-Approval Monitors
468582019-02-062663
34 Quality Assurance Committees
462622019-01-223034
35 Post-Approval Monitoring Program
462612018-09-068216
36 UW HRPP Quality Assurance
462602019-02-062631
37 IRB Purview
422732019-08-234223
38 Certificate of Confidentiality (CoC) Application Help
360922019-03-088058
39 Engagement in Human Participants Research at UW–Madison
355142019-10-0228135
40 IRB Meeting Minutes and Regulatory Documentation
355112019-01-223437

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