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Topics Map > Research Policy and Compliance > Human Research Protection Program (HRPP)
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No.Document TitleIDUpdatedHits
1 Human Subjects Research Protection Program (HRPP) Policy Index
341012019-11-1447807
2 Use of Human Fetal Tissue in Research
289972019-11-145475
3 Compliance with Human Research Protections in Sponsored Research
295542019-11-122969
4 Monitoring the Consent Process
295632019-11-123465
5 Exceptions to Informed Consent Requirements in Emergency Situations
295622019-11-122852
6 IRB Meetings
294672019-11-123490
7 Principal Investigator Status for UW–Madison Studies Involving Human Participants
295572019-11-1210761
8 Contact Information for Reporting Suggestions and Concerns
568892019-11-113790
9 Reporting of Suggestions and Concerns Regarding the Protection of Research Participants
292312019-11-113747
10 Good Clinical Practice (GCP) Training Guidance and Instructions
611352019-10-1711282
11 UW–Madison Federalwide Assurance (FWA) & IRB Registration Numbers
340482019-10-077545
12 Engagement in Human Participants Research at UW–Madison
355142019-10-0228170
13 HRPP Guidance, Forms and Resources
341022019-10-0112157
14 Good Clinical Practice (GCP) Refresher Instructions
624332019-09-234159
15 Instructions for Completing CITI Refresher Training
608382019-09-2315658
16 Clinical Trials Registration & Results Reporting
340442019-08-2948737
17 Initial Review: Submission and Review Policy
289372019-08-235284
18 IRB Purview
422732019-08-234240
19 Additional Requirements When Conducting Human Subjects Research with Environmental Protection Agency (EPA) Support
555332019-08-192918
20 Additional Requirements When Conducting Human Subjects Research with Department of Energy (DOE) Support
555892019-08-053071

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