Results: 1–20 of 125

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NumberDocument TitleIDUpdatedViews
1Instructions for Linking Previous CITI Training to Your NetID327242024-10-1865804
2Obtaining and Documenting Informed Consent297622024-10-1813824
3Monitoring the Consent Process295632024-10-187257
4Maintenance of IRB Records294762024-10-187631
5IRB Review of Study Resources291672024-10-186311
6IRB Reliance295652024-10-1811795
7IRB Purview422732024-10-188916
8IRB Members’ Conflicts of Interest294662024-10-1811146
9Reporting to Institutional and External Authorities291782024-10-188966
10Initial Review: Submission and Review Policy289372024-10-1810124
11HRPP and IRB Resources291642024-10-186554
12Exempt Research291742024-10-1813887
13Engagement in Human Participants Research at UW–Madison355142024-10-1835471
14Instructions for Completing CITI Human Participants Research Training325592024-10-18196094
15Good Clinical Practice (GCP) Training Guidance and Instructions611352024-10-1825611
16Good Clinical Practice (GCP) Refresher Instructions624332024-10-1812820
17HRPP Guidance, Forms and Resources341022024-10-1823586
18Developing an Internal Quality Assurance (QA) Program Guidance695542024-10-1812141
19Certificate of Confidentiality (CoC) Application Help360922024-10-1815913
20Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642024-10-1818564

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