Results: 1-20 of 67

No.Document TitleIDUpdatedViews
1Recruitment of Research Participants Guidance295602024-10-1817626
2ED/SBS IRB Principal Investigator Responsibilities557692024-10-186440
3Contact Information for Reporting Suggestions and Concerns568892024-10-189687
4Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186941
5Use of Human Fetal Tissue in Research289972024-10-1812645
6Unanticipated Problems295062024-10-1810454
7Suspension and Termination of Approved Research295222024-10-189367
8Study Closure506222024-10-1810450
9Student Research291682024-10-1810112
10Research with Adult Participants Lacking Capacity to Consent295452024-10-1813717
11Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188801
12Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823108
13Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818915
14Noncompliance295072024-10-1819148
15Obtaining and Documenting Informed Consent297622024-10-1813644
16Monitoring the Consent Process295632024-10-187087
17Maintenance of IRB Records294762024-10-187469
18IRB Review of Study Resources291672024-10-186164
19IRB Reliance295652024-10-1811636
20IRB Purview422732024-10-188749

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