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Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
1 Principal Investigator Status for UW–Madison Studies Involving Human Participants
295572019-01-168815
2 Clinical Trials Registration & Results Reporting
340442019-01-1546266
3 Compliance Monitoring and Quality Improvement
295472019-01-024672
4 IRB Composition and Quality Performance
294642019-01-023093
5 Obtaining and Documenting Informed Consent
297622019-01-026562
6 IRB Members’ Conflicts of Interest
294662019-01-024790
7 UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
340482018-11-276021
8 Human Subjects Research Protection Program (HRPP) Policy Index
341012018-10-0243356
9 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642018-10-013679
10 Review of Research Involving Vulnerable Participants
297612018-10-0110103
11 Recruitment of Research Participants Guidance
295602018-10-017150
12 Instructions for Linking Previous CITI Training to Your NetID
327242018-10-0143306
13 Research with Adult Participants Lacking Capacity to Consent
295452018-10-014568
14 Good Clinical Practice (GCP) Training Guidance and Instructions
611352018-09-268638
15 Instructions for Completing CITI Human Participants Research Training
325592018-09-25173165
16 HRPP Guidance, Forms and Resources
341022018-09-2110141
17 Research Participants
341002018-09-173788
18 Cross-Campus Human Research Protection Program (HRPP) Committee Charter
297912018-09-143620
19 Post-Approval Monitoring Program
462612018-09-066829
20 Issues in Human Subjects Research When State Law May Apply
295462018-08-288375

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