Results: 1-20 of 68

No.Document TitleIDUpdatedViews
1Recruitment of Research Participants Guidance295602024-10-1817374
2ED/SBS IRB Principal Investigator Responsibilities557692024-10-186157
3Contact Information for Reporting Suggestions and Concerns568892024-10-189418
4Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186659
5Use of Human Fetal Tissue in Research289972024-10-1812290
6Unanticipated Problems295062024-10-1810237
7Suspension and Termination of Approved Research295222024-10-189166
8Study Closure506222024-10-1810177
9Student Research291682024-10-189858
10Research with Adult Participants Lacking Capacity to Consent295452024-10-1813332
11Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-188562
12Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822759
13Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1818500
14Noncompliance295072024-10-1818851
15Obtaining and Documenting Informed Consent297622024-10-1813387
16Monitoring the Consent Process295632024-10-186913
17Maintenance of IRB Records294762024-10-187180
18IRB Review of Study Resources291672024-10-185980
19IRB Reliance295652024-10-1811361
20IRB Purview422732024-10-188486
1  2  3  4  Next

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