Results: 1-20 of 81

No.Document TitleIDUpdatedViews
1Good Clinical Practice (GCP) Training Guidance and Instructions611352024-01-1123142
2HRPP Guidance, Forms and Resources341022023-09-2721606
3Clinical Trials Registration & Results Reporting340442023-09-1858475
4UW Post-Approval Monitors468582023-08-095728
5Certificate of Confidentiality (CoC) Application Help360922023-05-1113508
6UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers340482022-10-2614828
7Post Approval Monitoring Program Services628712022-04-184820
8Post-Approval Monitoring Program462612022-04-1114775
9Instructions for Linking Previous CITI Training to Your NetID327242022-01-2863133
10Contact Information for Reporting Suggestions and Concerns568892022-01-288268
11Issues in Human Subjects Research When State Law May Apply295462022-01-2719387
12Instructions for Completing CITI Refresher Training608382021-10-2027449
13Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642021-08-0916374
14Preventing Noncompliance Guidance693702021-08-0911099
15Developing an Internal Quality Assurance (QA) Program Guidance695542021-08-0910375
16Recruitment of Research Participants Guidance295602021-02-0316083
17Human Subjects Research Protection Program (HRPP) Policy Index341012020-11-3053448
18Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992020-11-305915
19Use of Human Fetal Tissue in Research289972020-11-2510264
20Unanticipated Problems295062020-11-259288
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