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Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
1 Post Approval Monitoring Program Services
628712022-04-183771
2 Good Clinical Practice (GCP) Training Guidance and Instructions
611352022-04-1518234
3 Post-Approval Monitoring Program
462612022-04-1111875
4 Certificate of Confidentiality (CoC) Application Help
360922022-04-0811359
5 UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
340482022-03-3011745
6 Instructions for Linking Previous CITI Training to Your NetID
327242022-01-2860443
7 Contact Information for Reporting Suggestions and Concerns
568892022-01-286487
8 Issues in Human Subjects Research When State Law May Apply
295462022-01-2715216
9 HRPP Guidance, Forms and Resources
341022022-01-1318717
10 Instructions for Completing CITI Refresher Training
608382021-10-2026126
11 Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance
695642021-08-0913322
12 Preventing Noncompliance Guidance
693702021-08-098697
13 Developing an Internal Quality Assurance (QA) Program Guidance
695542021-08-097623
14 Recruitment of Research Participants Guidance
295602021-02-0313691
15 Clinical Trials Registration & Results Reporting
340442020-12-2354709
16 Human Subjects Research Protection Program (HRPP) Policy Index
341012020-11-3052080
17 Reporting of Suggestions and Concerns Regarding HRPP Performance and Function
557992020-11-304767
18 Use of Human Fetal Tissue in Research
289972020-11-258639
19 Unanticipated Problems
295062020-11-258194
20 Suspension and Termination of Approved Research
295222020-11-257116

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