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Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
1 Good Clinical Practice (GCP) Training Guidance and Instructions
611352019-10-1710955
2 UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
340482019-10-077372
3 Engagement in Human Participants Research at UW–Madison
355142019-10-0227924
4 Principal Investigator Status for UW–Madison Studies Involving Human Participants
295572019-10-0110499
5 HRPP Guidance, Forms and Resources
341022019-10-0111892
6 Good Clinical Practice (GCP) Refresher Instructions
624332019-09-234021
7 Instructions for Completing CITI Refresher Training
608382019-09-2315166
8 Clinical Trials Registration & Results Reporting
340442019-08-2948478
9 Human Subjects Research Protection Program (HRPP) Policy Index
341012019-08-2347524
10 Initial Review: Submission and Review Policy
289372019-08-235149
11 IRB Purview
422732019-08-234106
12 Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
555332019-08-192818
13 Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
555892019-08-052949
14 Application of Federalwide Assurance (FWA) Terms to UW-Madison Human Participants Research Policy
295522019-08-053502
15 Additional Requirements When Conducting Human Subjects Research with Department of Education (ED) Support
548022019-08-053049
16 Additional Requirements When Conducting Human Subjects Research with Department of Justice (DOJ) Support
547972019-08-052963
17 Additional Requirements When Conducting Human Subjects Research with Department of Defense (DOD) Support
531652019-06-243914
18 Compliance Monitoring and Quality Improvement
295472019-05-305764
19 Research with Adult Participants Lacking Capacity to Consent
295452019-05-035831
20 Obtaining and Documenting Informed Consent
297622019-05-037981

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