Results: 1–20 of 67

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NumberDocument TitleIDUpdatedViews
1Recruitment of Research Participants Guidance295602024-10-1817759
2ED/SBS IRB Principal Investigator Responsibilities557692024-10-186589
3Contact Information for Reporting Suggestions and Concerns568892024-10-189809
4Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-187090
5Use of Human Fetal Tissue in Research289972024-10-1812827
6Unanticipated Problems295062024-10-1810578
7Suspension and Termination of Approved Research295222024-10-189508
8Study Closure506222024-10-1810578
9Student Research291682024-10-1810448
10Research with Adult Participants Lacking Capacity to Consent295452024-10-1813871
11Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188946
12Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823267
13Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1819101
14Noncompliance295072024-10-1819282
15Obtaining and Documenting Informed Consent297622024-10-1813795
16Monitoring the Consent Process295632024-10-187215
17Maintenance of IRB Records294762024-10-187603
18IRB Review of Study Resources291672024-10-186286
19IRB Reliance295652024-10-1811761
20IRB Purview422732024-10-188888

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