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Document Title
ID
Updated
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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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