Results: 1–20 of 125

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NumberDocument TitleIDUpdatedViews
1Good Clinical Practice (GCP) Refresher Instructions624332024-10-1812839
2Noncompliance295072024-10-1819332
3Obtaining and Documenting Informed Consent297622024-10-1813841
4Monitoring the Consent Process295632024-10-187269
5Maintenance of IRB Records294762024-10-187643
6IRB Review of Study Resources291672024-10-186323
7IRB Reliance295652024-10-1811811
8IRB Purview422732024-10-188933
9IRB Members’ Conflicts of Interest294662024-10-1811164
10Reporting to Institutional and External Authorities291782024-10-188981
11Initial Review: Submission and Review Policy289372024-10-1810134
12HRPP and IRB Resources291642024-10-186566
13Exempt Research291742024-10-1813903
14Engagement in Human Participants Research at UW–Madison355142024-10-1835483
15Instructions for Completing CITI Human Participants Research Training325592024-10-18196148
16Good Clinical Practice (GCP) Training Guidance and Instructions611352024-10-1825625
17Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642024-10-1818588
18HRPP Guidance, Forms and Resources341022024-10-1823606
19Developing an Internal Quality Assurance (QA) Program Guidance695542024-10-1812153
20List of Approved De-Identified Publicly Available Datasets295502024-10-1811704

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