Results: 1-20 of 44

No.Document TitleIDUpdatedViews
1ED/SBS IRB Principal Investigator Responsibilities557692024-10-185630
2Reporting of Suggestions and Concerns Regarding HRPP Performance and Function557992024-10-186302
3Use of Human Fetal Tissue in Research289972024-10-1811510
4Unanticipated Problems295062024-10-189672
5Suspension and Termination of Approved Research295222024-10-188602
6Study Closure506222024-10-189770
7Student Research291682024-10-189385
8Research with Adult Participants Lacking Capacity to Consent295452024-10-1812261
9Reporting of Suggestions and Concerns Regarding the Protection of Research Participants292312024-10-187993
10Protecting Research Participants Privacy Interests and Confidentiality of Data295612024-10-1822232
11Principal Investigator Status for UW–Madison Studies Involving Human Participants295572024-10-1817929
12Noncompliance295072024-10-1818361
13Obtaining and Documenting Informed Consent297622024-10-1812994
14Monitoring the Consent Process295632024-10-186564
15Maintenance of IRB Records294762024-10-186826
16IRB Review of Study Resources291672024-10-185685
17IRB Reliance295652024-10-1810885
18IRB Purview422732024-10-188079
19IRB Members’ Conflicts of Interest294662024-10-1810133
20Reporting to Institutional and External Authorities291782024-10-187726
1  2  3  Next

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