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Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
1 Single Institutional Review Board (IRB) for Multi-Site Federal Grants Policy
739912020-11-245773
2 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642021-08-0915734
3 Developing an Internal Quality Assurance (QA) Program Guidance
695542021-08-099646
4 Preventing Noncompliance Guidance
693702021-08-0910533
5 Human Research Protection Program (HRPP) Newsletter - Fall 2016
686262020-04-024598
6 Post Approval Monitoring Program Services
628712022-04-184590
7 Good Clinical Practice (GCP) Refresher Instructions
624332020-04-029882
8 Human Research Protection Program (HRPP) Newsletter - Spring 2016
624012020-04-024500
9 Good Clinical Practice (GCP) Training Guidance and Instructions
611352022-04-1521748
10 Instructions for Completing CITI Refresher Training
608382021-10-2027146
11 Reportable Abuse and Neglect Guidance
591102017-10-035465
12 UW Human Research Protection Program Newsletter - Fall 2015
568972020-04-024326
13 Contact Information for Reporting Suggestions and Concerns
568892022-01-287774
14 Human Research Protection Program Newsletter
565352020-04-025165
15 Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
557992020-11-305650
16 OPRR Guidance on 45 CFR 46.101(b)(5): Exemption for Research and Demonstration Projects on Public Benefit and Service Programs
557722017-10-034518
17 UW-Madison HIPAA Program
557702017-10-034535
18 ED/SBS IRB Principal Investigator Responsibilities
557692018-02-074998
19 FDA IRB Regulations (21 CFR 56)
544892017-10-034801
20 Common Rule (45 CFR 46)
544882017-10-035408

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