Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results : 41-60 of 81
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No.Document TitleIDUpdatedHits
41 IRB Meetings
294672020-11-246133
42 IRB Meeting Minutes and Regulatory Documentation
355112020-11-246129
43 IRB Consultants Use and Conflict of Interest
294602017-10-036222
44 IRB Composition and Quality Performance
294642020-11-246826
45 IRB Authority and Independence
291692019-01-227687
46 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642021-08-0915745
47 Instructions for Linking Previous CITI Training to Your NetID
327242022-01-2862553
48 Instructions for Completing CITI Refresher Training
608382021-10-2027152
49 Instructions for Completing CITI Human Participants Research Training
325592018-09-25190713
50 Institutional Official in Charge of HRPP
291632020-11-247503
51 Initial Review: Submission and Review Policy
289372020-11-238714
52 Human Subjects Research Protection Program (HRPP) Policy Index
341012020-11-3053162
53 Human Research Protection Program Newsletter
565352020-04-025168
54 HRPP Guidance, Forms and Resources
341022023-09-2220833
55 HRPP Education and Training
288992020-11-237660
56 HRPP and IRB Resources
291642020-11-235395
57 Good Clinical Practice (GCP) Training Guidance and Instructions
611352022-04-1521765
58 FDA IRB Regulations (21 CFR 56)
544892017-10-034804
59 Exempt Research
291742020-11-2312337
60 Exceptions to Informed Consent Requirements in Emergency Situations
295622020-11-235238

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