Results: 1–20 of 125

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Search results updated. Showing 20 documents in Table format.
NumberDocument TitleIDUpdatedViews
1Instructions for Linking Previous CITI Training to Your NetID327242024-10-1865785
2Obtaining and Documenting Informed Consent297622024-10-1813804
3Monitoring the Consent Process295632024-10-187223
4Maintenance of IRB Records294762024-10-187610
5IRB Review of Study Resources291672024-10-186293
6IRB Reliance295652024-10-1811769
7IRB Purview422732024-10-188895
8IRB Members’ Conflicts of Interest294662024-10-1811130
9Reporting to Institutional and External Authorities291782024-10-188949
10Initial Review: Submission and Review Policy289372024-10-1810104
11HRPP and IRB Resources291642024-10-186539
12Exempt Research291742024-10-1813865
13Engagement in Human Participants Research at UW–Madison355142024-10-1835451
14Instructions for Completing CITI Human Participants Research Training325592024-10-18196047
15Good Clinical Practice (GCP) Training Guidance and Instructions611352024-10-1825585
16Good Clinical Practice (GCP) Refresher Instructions624332024-10-1812794
17HRPP Guidance, Forms and Resources341022024-10-1823550
18Developing an Internal Quality Assurance (QA) Program Guidance695542024-10-1812116
19Certificate of Confidentiality (CoC) Application Help360922024-10-1815891
20Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642024-10-1818536

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