Results: 1-20 of 69

No.Document TitleIDUpdatedViews
1Clinical Trials Registration & Results Reporting340442024-07-2259292
2Certificate of Confidentiality (CoC) Application Help360922024-06-1814785
3Good Clinical Practice (GCP) Training Guidance and Instructions611352024-01-1124191
4HRPP Guidance, Forms and Resources341022023-09-2722210
5UW Post-Approval Monitors468582023-08-095996
6UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers340482022-10-2615472
7Post Approval Monitoring Program Services628712022-04-185030
8Post-Approval Monitoring Program462612022-04-1115406
9Instructions for Linking Previous CITI Training to Your NetID327242022-01-2863767
10Contact Information for Reporting Suggestions and Concerns568892022-01-288628
11Issues in Human Subjects Research When State Law May Apply295462022-01-2721305
12Instructions for Completing CITI Refresher Training608382021-10-2027673
13Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642021-08-0916964
14Preventing Noncompliance Guidance693702021-08-0911490
15Developing an Internal Quality Assurance (QA) Program Guidance695542021-08-0911030
16Recruitment of Research Participants Guidance295602021-02-0316355
17Human Subjects Research Protection Program (HRPP) Policy Index341012020-11-3053749
18Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992020-11-306143
19Use of Human Fetal Tissue in Research289972020-11-2511003
20Unanticipated Problems295062020-11-259494
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