Results: 21-40 of 66
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No.Document TitleIDUpdatedHits
21 How to Conduct PRS Review
205772017-08-186120
22 Making a Motion at IRB Meetings
315232017-08-114734
23 Reviewing Initial Applications In ARROW
192132017-08-074170
24 Drugs, Biologics, and Devices: Regulations
192412017-07-287717
25 Informed Consent Process, Elements, and Waivers
192312017-07-148023
26 New IRB Members Guide
246842017-05-224976
27 IRB Member Newsletter--Volume 8 (Winter 2013)
361052017-04-184443
28 IRB Member Newsletter--Volume 7 (Spring 2013)
297472017-04-184065
29 Primary Reviewer Guidance for Initial Reviews
196832017-03-277410
30 Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications
217712017-03-277865
31 Overview of the Accreditation Process and UW-Madison's Human Research Protections Program
192362017-02-155765
32 IRB Member Newsletter--Volume 2 (Winter 2010)
191942017-01-303530
33 Finding Study-Related Documents in ARROW
192142017-01-235930
34 Cheat Sheet (w/ screenshots) for Initial Reviews in ARROW
192162017-01-234479
35 Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
192282017-01-236150
36 IRB Member Newsletter--Volume 1 (Fall 2009)
191932017-01-183472
37 Continuing Review & Changes of Protocol
192292017-01-188035
38 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-188684
39 Belmont Report
192002017-01-0639100
40 IRB Member Newsletter--Volume 5 (Spring/Summer 2012)
246302017-01-054417

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