Search result for "": 1-20

No.	Document Title	ID	Updated	Hits
1	Belmont Report	19200	2017-01-06	41815
2	Noncompliance, Protocol Exceptions and Deviations	19235	2018-01-23	36283
3	For IRB Members	19119	2021-03-09	32600
4	Unanticipated Problems and Serious Adverse Events	19243	2016-12-27	20020
5	Genetic Testing or Analysis	19770	2017-11-27	18516
6	Prisoners: Regulations	19240	2016-12-27	11671
7	Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)	19230	2017-01-18	9691
8	Continuing Review & Changes of Protocol	19229	2017-01-18	9214
9	Informed Consent Process, Elements, and Waivers	19231	2017-07-14	8960
10	Privacy & Confidentiality	19237	2019-08-05	8939
11	Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications	21771	2017-03-27	8913
12	Primary Reviewer Guidance for Initial Reviews	19683	2017-03-27	8806
13	Drugs, Biologics, and Devices: Regulations	19241	2017-07-28	8636
14	Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance	19232	2019-03-07	8171
15	Reviewing IRB Meeting Minutes in ARROW	19227	2016-01-19	7268
16	Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities	19228	2017-01-23	7185
17	How to Conduct PRS Review	20577	2017-08-18	7137
18	Brief Responsibilities of an MR-IRB Member	19206	2020-06-02	7050
19	Finding Study-Related Documents in ARROW	19214	2017-01-23	6973
20	Meeting Workspace Navigation Guide for IRB Members	20587	2016-12-19	6934

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