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Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
Results: 1-20 of 91
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No.Document TitleIDUpdatedHits
1 Developing an Internal Quality Assurance (QA) Program Guidance
695542021-05-125888
2 Preventing Noncompliance Guidance
693702021-05-126765
3 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642021-05-1210613
4 Good Clinical Practice (GCP) Training Guidance and Instructions
611352021-05-1115004
5 Certificate of Confidentiality (CoC) Application Help
360922021-04-029972
6 HRPP Guidance, Forms and Resources
341022021-02-2615968
7 Recruitment of Research Participants Guidance
295602021-02-0311608
8 Clinical Trials Registration & Results Reporting
340442020-12-2352046
9 Human Subjects Research Protection Program (HRPP) Policy Index
341012020-11-3050632
10 Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
557992020-11-303837
11 Use of Human Fetal Tissue in Research
289972020-11-257423
12 Unanticipated Problems
295062020-11-257152
13 Suspension and Termination of Approved Research
295222020-11-256130
14 Study Closure
506222020-11-257016
15 Student Research
291682020-11-246845
16 Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
739912020-11-244131
17 Review of Data and Safety Monitoring in Research
294972020-11-244860
18 Review of Research Involving Vulnerable Participants
297612020-11-2420187
19 Retention of IRB Records
294772020-11-246215
20 Research with Adult Participants Lacking Capacity to Consent
295452020-11-248490
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