Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results: 21-40 of 99
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No.Document TitleIDUpdatedHits
21 Evaluating the Scientific or Scholarly Merits of Proposed Research
291552018-04-094649
22 Equitable Selection of Research Participants Guidance
295592018-04-094728
23 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642018-04-062279
24 Exempt Research
291742018-04-064706
25 Certificate of Confidentiality (CoC) Application Help
360922018-04-065368
26 Post-Approval Monitoring Program
462612018-04-056057
27 Good Clinical Practice (GCP) Training Guidance and Instructions
611352018-04-047375
28 Human Participants Research Training
340452018-04-0313505
29 Recruitment of Research Participants Guidance
295602018-04-026346
30 Review of Research Involving Vulnerable Participants
297612018-04-027275
31 Instructions for Completing CITI Refresher Training
608382018-03-299561
32 IRB Members’ Conflicts of Interest
294662018-03-284316
33 Obtaining and Documenting Informed Consent
297622018-03-286050
34 Clinical Trials Registration & Results Reporting
340442018-03-2845081
35 Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
555332018-03-211674
36 Creation and Dissemination of Policies and Related Documentation
297562018-03-122661
37 Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
295522018-02-192446
38 Exempt Research (for non-federally funded, non-FDA-regulated, non-VA research)
799602018-02-19470
39 Research with Adult Participants Lacking Capacity to Consent
295452018-02-194006
40 De-Identified Publicly Available Datasets Guidance
294652018-02-074844

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