Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
21 Considerations for Accepting or Ceding IRB Review Guidance
566202017-10-033297
22 Contact Information for Reporting Suggestions and Concerns
568892019-11-114742
23 Continuing Review: Submission and Review
297582020-11-238378
24 Creation and Dissemination of Policies and Related Documentation
297562020-11-234802
25 Cross-Campus Human Research Protection Program (HRPP) Committee Charter
297912020-11-235239
26 De-Identified Publicly Available Datasets Guidance
294652018-02-077681
27 Developing an Internal Quality Assurance (QA) Program Guidance
695542017-10-035276
28 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-072734
29 Engagement in Human Participants Research at UW–Madison
355142020-11-2330191
30 Equitable Selection of Research Participants Guidance
295592018-04-098318
31 Exceptions to Informed Consent Requirements in Emergency Situations
295622020-11-233623
32 Exempt Research
291742020-11-239136
33 FDA IRB Regulations (21 CFR 56)
544892017-10-032863
34 Good Clinical Practice (GCP) Training Guidance and Instructions
611352020-04-0213716
35 HRPP and IRB Resources
291642020-11-233767
36 HRPP Education and Training
288992020-11-235836
37 HRPP Guidance, Forms and Resources
341022020-10-1514793
38 HRPP Newsletter - Spring 2018
822752018-05-161614
39 Human Research Protection Program Newsletter
565352020-04-023215
40 Human Subjects Research Protection Program (HRPP) Policy Index
341012020-07-1049970

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