Results: 1-20 of 68

No.Document TitleIDUpdatedViews
1Recruitment of Research Participants Guidance295602024-10-1817559
2ED/SBS IRB Principal Investigator Responsibilities557692024-10-186356
3Contact Information for Reporting Suggestions and Concerns568892024-10-189624
4Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186882
5Use of Human Fetal Tissue in Research289972024-10-1812576
6Unanticipated Problems295062024-10-1810409
7Suspension and Termination of Approved Research295222024-10-189307
8Study Closure506222024-10-1810381
9Student Research291682024-10-1810062
10Research with Adult Participants Lacking Capacity to Consent295452024-10-1813630
11Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188750
12Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1823029
13Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818811
14Noncompliance295072024-10-1819093
15Obtaining and Documenting Informed Consent297622024-10-1813572
16Monitoring the Consent Process295632024-10-187049
17Maintenance of IRB Records294762024-10-187400
18IRB Review of Study Resources291672024-10-186111
19IRB Reliance295652024-10-1811567
20IRB Purview422732024-10-188679

Not finding what you are looking for? Suggest a new document be created, or try adjusting your search criteria.