Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results : 21-40 of 91
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No.Document TitleIDUpdatedHits
21 Recruitment of Research Participants Guidance
295602021-02-0313864
22 Protecting Research Participants Privacy Interests and Confidentiality of Data
295612020-11-2420564
23 Principal Investigator Status for UW–Madison Studies Involving Human Participants
295572020-11-2415732
24 Preventing Noncompliance Guidance
693702021-08-098867
25 Post-Approval Monitoring Program
462612022-04-1112005
26 Post Approval Monitoring Program Services
628712022-04-183854
27 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-033804
28 OHRP Guidance on Engagement of Institutions in Human Subjects Research
497932017-10-034437
29 Office for Human Research Protections (OHRP) - IRB Knowledge of Local Research Context
507842017-10-033966
30 Obtaining and Documenting Informed Consent
297622020-11-2411377
31 Noncompliance
295072020-11-2416387
32 NIH Genomic Data Sharing Policy for Human Data Guidance
495782017-10-035382
33 Monitoring the Consent Process
295632020-11-245542
34 Maintenance of IRB Records
294762020-11-245682
35 List of Approved De-Identified Publicly Available Datasets
295502017-10-038353
36 Issues in Human Subjects Research When State Law May Apply
295462022-01-2715431
37 IRB Review of Study Resources
291672020-11-244550
38 IRB Reliance
295652020-11-249348
39 IRB Purview
422732020-11-246741
40 IRB Members’ Conflicts of Interest
294662020-11-248670

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