Results: 1–20 of 125

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NumberDocument TitleIDUpdatedViews
1Instructions for Linking Previous CITI Training to Your NetID327242024-10-1865787
2Obtaining and Documenting Informed Consent297622024-10-1813805
3Monitoring the Consent Process295632024-10-187226
4Maintenance of IRB Records294762024-10-187611
5IRB Review of Study Resources291672024-10-186295
6IRB Reliance295652024-10-1811771
7IRB Purview422732024-10-188897
8IRB Members’ Conflicts of Interest294662024-10-1811131
9Reporting to Institutional and External Authorities291782024-10-188950
10Initial Review: Submission and Review Policy289372024-10-1810106
11HRPP and IRB Resources291642024-10-186541
12Exempt Research291742024-10-1813866
13Engagement in Human Participants Research at UW–Madison355142024-10-1835452
14Instructions for Completing CITI Human Participants Research Training325592024-10-18196049
15Good Clinical Practice (GCP) Training Guidance and Instructions611352024-10-1825588
16Good Clinical Practice (GCP) Refresher Instructions624332024-10-1812796
17HRPP Guidance, Forms and Resources341022024-10-1823554
18Developing an Internal Quality Assurance (QA) Program Guidance695542024-10-1812117
19Certificate of Confidentiality (CoC) Application Help360922024-10-1815892
20Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642024-10-1818538

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