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Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
1 Instructions for Linking Previous CITI Training to Your NetID
327242019-12-3053758
2 Certificate of Confidentiality (CoC) Application Help
360922019-12-198398
3 Clinical Trials Registration & Results Reporting
340442019-12-0449210
4 Human Subjects Research Protection Program (HRPP) Policy Index
341012019-11-1448229
5 Use of Human Fetal Tissue in Research
289972019-11-145725
6 Compliance with Human Research Protections in Sponsored Research
295542019-11-123105
7 Monitoring the Consent Process
295632019-11-123664
8 Exceptions to Informed Consent Requirements in Emergency Situations
295622019-11-123012
9 IRB Meetings
294672019-11-123661
10 Principal Investigator Status for UW–Madison Studies Involving Human Participants
295572019-11-1211143
11 Contact Information for Reporting Suggestions and Concerns
568892019-11-113982
12 Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
292312019-11-114027
13 Good Clinical Practice (GCP) Training Guidance and Instructions
611352019-10-1711747
14 UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
340482019-10-077860
15 Engagement in Human Participants Research at UW–Madison
355142019-10-0228516
16 HRPP Guidance, Forms and Resources
341022019-10-0112583
17 Good Clinical Practice (GCP) Refresher Instructions
624332019-09-234435
18 Instructions for Completing CITI Refresher Training
608382019-09-2316406
19 Initial Review: Submission and Review Policy
289372019-08-235481
20 IRB Purview
422732019-08-234430

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