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No.Document TitleIDUpdatedHits
1 For IRB Members
191192020-06-0229935
2 IRB Member Newsletter--Volume 1 (Fall 2009)
191932017-01-183338
3 IRB Member Newsletter--Volume 2 (Winter 2010)
191942017-01-303425
4 Brief Responsibilities of an HS-IRB Member
191992020-06-025342
5 Belmont Report
192002017-01-0638251
6 Brief Responsibilities of an MR-IRB Member
192062020-06-025901
7 Reviewing Initial Applications In ARROW
192132017-08-073993
8 Finding Study-Related Documents in ARROW
192142017-01-235692
9 Cheat Sheet (w/ screenshots) for Initial Reviews in ARROW
192162017-01-234318
10 Initial Review Tips for IRB Members
192262018-03-194410
11 Reviewing IRB Meeting Minutes in ARROW
192272016-01-196186
12 Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
192282017-01-235937
13 Continuing Review & Changes of Protocol
192292017-01-187739
14 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-188457
15 Informed Consent Process, Elements, and Waivers
192312017-07-147681
16 Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance
192322019-03-077157
17 Noncompliance, Protocol Exceptions and Deviations
192352018-01-2333628
18 Overview of the Accreditation Process and UW-Madison's Human Research Protections Program
192362017-02-155614
19 Privacy & Confidentiality
192372019-08-057725
20 Children as research participants: Regulations
192382018-12-044220

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