Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results: 21-40 of 99
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No.Document TitleIDUpdatedHits
21 Post-Approval Monitoring Program
462612018-04-055571
22 Good Clinical Practice (GCP) Training Guidance and Instructions
611352018-04-046734
23 Principal Investigator Status for UW–Madison Studies Involving Human Participants
295572018-04-047306
24 Human Participants Research Training
340452018-04-0312942
25 Recruitment of Research Participants Guidance
295602018-04-025962
26 Review of Research Involving Vulnerable Participants
297612018-04-026498
27 HRPP Guidance, Forms and Resources
341022018-03-298599
28 Instructions for Completing CITI Refresher Training
608382018-03-298508
29 IRB Members’ Conflicts of Interest
294662018-03-284072
30 Obtaining and Documenting Informed Consent
297622018-03-285801
31 Clinical Trials Registration & Results Reporting
340442018-03-2844451
32 Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
555332018-03-211473
33 Creation and Dissemination of Policies and Related Documentation
297562018-03-122515
34 Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
295522018-02-192288
35 Study Closure
506222018-02-192722
36 Exempt Research (for non-federally funded, non-FDA-regulated, non-VA research)
799602018-02-19291
37 Research with Adult Participants Lacking Capacity to Consent
295452018-02-193740
38 De-Identified Publicly Available Datasets Guidance
294652018-02-074624
39 IRB Composition and Quality Performance
294642018-02-072612
40 Reporting to Institutional and External Authorities
291782018-02-072605

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