Results: 1-20 of 68

No.Document TitleIDUpdatedViews
1Recruitment of Research Participants Guidance295602024-10-1817413
2ED/SBS IRB Principal Investigator Responsibilities557692024-10-186211
3Contact Information for Reporting Suggestions and Concerns568892024-10-189494
4Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186716
5Use of Human Fetal Tissue in Research289972024-10-1812353
6Unanticipated Problems295062024-10-1810268
7Suspension and Termination of Approved Research295222024-10-189188
8Study Closure506222024-10-1810212
9Student Research291682024-10-189900
10Research with Adult Participants Lacking Capacity to Consent295452024-10-1813408
11Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188608
12Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822845
13Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818586
14Noncompliance295072024-10-1818916
15Obtaining and Documenting Informed Consent297622024-10-1813414
16Monitoring the Consent Process295632024-10-186933
17Maintenance of IRB Records294762024-10-187238
18IRB Review of Study Resources291672024-10-186008
19IRB Reliance295652024-10-1811406
20IRB Purview422732024-10-188518
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