Search result for "": 1-20

No.	Document Title	ID	Updated	Hits
1	Belmont Report	19200	2017-01-06	38694
2	Noncompliance, Protocol Exceptions and Deviations	19235	2018-01-23	33922
3	For IRB Members	19119	2020-06-02	30179
4	Unanticipated Problems and Serious Adverse Events	19243	2016-12-27	17902
5	Genetic Testing or Analysis	19770	2017-11-27	16643
6	Prisoners: Regulations	19240	2016-12-27	10683
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	8555
8	Continuing Review & Changes of Protocol	19229	2017-01-18	7899
9	Privacy & Confidentiality	19237	2019-08-05	7858
10	Informed Consent Process, Elements, and Waivers	19231	2017-07-14	7834
11	Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications	21771	2017-03-27	7739
12	Drugs, Biologics, and Devices: Regulations	19241	2017-07-28	7574
13	Primary Reviewer Guidance for Initial Reviews	19683	2017-03-27	7234
14	Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance	19232	2019-03-07	7229
15	Reviewing IRB Meeting Minutes in ARROW	19227	2016-01-19	6267
16	Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities	19228	2017-01-23	6024
17	How to Conduct PRS Review	20577	2017-08-18	6000
18	Brief Responsibilities of an MR-IRB Member	19206	2020-06-02	5982
19	Meeting Workspace Navigation Guide for IRB Members	20587	2016-12-19	5943
20	Finding Study-Related Documents in ARROW	19214	2017-01-23	5772

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