Results: 1-20 of 69

No.Document TitleIDUpdatedViews
1Clinical Trials Registration & Results Reporting340442024-07-2259299
2Certificate of Confidentiality (CoC) Application Help360922024-06-1814789
3Good Clinical Practice (GCP) Training Guidance and Instructions611352024-01-1124200
4HRPP Guidance, Forms and Resources341022023-09-2722218
5UW Post-Approval Monitors468582023-08-096002
6UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers340482022-10-2615478
7Post Approval Monitoring Program Services628712022-04-185034
8Post-Approval Monitoring Program462612022-04-1115415
9Instructions for Linking Previous CITI Training to Your NetID327242022-01-2863778
10Contact Information for Reporting Suggestions and Concerns568892022-01-288634
11Issues in Human Subjects Research When State Law May Apply295462022-01-2721313
12Instructions for Completing CITI Refresher Training608382021-10-2027678
13Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642021-08-0916977
14Preventing Noncompliance Guidance693702021-08-0911497
15Developing an Internal Quality Assurance (QA) Program Guidance695542021-08-0911040
16Recruitment of Research Participants Guidance295602021-02-0316365
17Human Subjects Research Protection Program (HRPP) Policy Index341012020-11-3053755
18Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992020-11-306147
19Use of Human Fetal Tissue in Research289972020-11-2511014
20Unanticipated Problems295062020-11-259496
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