Results: 1–20 of 125

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NumberDocument TitleIDUpdatedViews
1Good Clinical Practice (GCP) Refresher Instructions624332024-10-1812940
2Noncompliance295072024-10-1819429
3Obtaining and Documenting Informed Consent297622024-10-1813934
4Monitoring the Consent Process295632024-10-187334
5Maintenance of IRB Records294762024-10-187723
6IRB Review of Study Resources291672024-10-186407
7IRB Reliance295652024-10-1811919
8IRB Purview422732024-10-189035
9IRB Members’ Conflicts of Interest294662024-10-1811271
10Reporting to Institutional and External Authorities291782024-10-189059
11Initial Review: Submission and Review Policy289372024-10-1810208
12HRPP and IRB Resources291642024-10-186616
13Exempt Research291742024-10-1813974
14Engagement in Human Participants Research at UW–Madison355142024-10-1835586
15Instructions for Completing CITI Human Participants Research Training325592024-10-18196357
16Good Clinical Practice (GCP) Training Guidance and Instructions611352024-10-1825709
17Investigating the Cause of Noncompliance and Implementing Corrective and Preventive Action (CAPA) Plans Guidance695642024-10-1818690
18HRPP Guidance, Forms and Resources341022024-10-1823716
19Developing an Internal Quality Assurance (QA) Program Guidance695542024-10-1812250
20List of Approved De-Identified Publicly Available Datasets295502024-10-1811781

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