Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results : 41-60 of 91
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No.Document TitleIDUpdatedHits
41 IRB Meetings
294672020-11-245420
42 IRB Meeting Minutes and Regulatory Documentation
355112020-11-245442
43 IRB Consultants Use and Conflict of Interest
294602017-10-035557
44 IRB Composition and Quality Performance
294642020-11-246107
45 IRB Authority and Independence
291692019-01-226820
46 IRB Analysis of Risks and Benefits of Research Guidance
294782017-10-039408
47 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642021-08-0913525
48 Instructions for Linking Previous CITI Training to Your NetID
327242022-01-2860683
49 Instructions for Completing CITI Refresher Training
608382021-10-2026221
50 Instructions for Completing CITI Human Participants Research Training
325592018-09-25188636
51 Institutional Official in Charge of HRPP
291632020-11-246778
52 Initial Review: Submission and Review Policy
289372020-11-237853
53 Human Subjects Research Protection Program (HRPP) Policy Index
341012020-11-3052174
54 Human Research Protection Program Newsletter
565352020-04-024506
55 HRPP Newsletter - Spring 2018
822752018-05-162537
56 HRPP Guidance, Forms and Resources
341022022-01-1318888
57 HRPP Education and Training
288992020-11-237018
58 HRPP and IRB Resources
291642020-11-234768
59 Good Clinical Practice (GCP) Training Guidance and Instructions
611352022-04-1518504
60 FDA IRB Regulations (21 CFR 56)
544892017-10-034049

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