Results: 21-40 of 65
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No.Document TitleIDUpdatedHits
21 Making a Motion at IRB Meetings
315232017-08-114556
22 Reviewing Initial Applications In ARROW
192132017-08-074075
23 Drugs, Biologics, and Devices: Regulations
192412017-07-287566
24 Informed Consent Process, Elements, and Waivers
192312017-07-147822
25 New IRB Members Guide
246842017-05-224868
26 IRB Member Newsletter--Volume 8 (Winter 2013)
361052017-04-184348
27 IRB Member Newsletter--Volume 7 (Spring 2013)
297472017-04-183942
28 Primary Reviewer Guidance for Initial Reviews
196832017-03-277220
29 Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications
217712017-03-277728
30 Overview of the Accreditation Process and UW-Madison's Human Research Protections Program
192362017-02-155668
31 IRB Member Newsletter--Volume 2 (Winter 2010)
191942017-01-303459
32 Finding Study-Related Documents in ARROW
192142017-01-235766
33 Cheat Sheet (w/ screenshots) for Initial Reviews in ARROW
192162017-01-234362
34 Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
192282017-01-236013
35 IRB Member Newsletter--Volume 1 (Fall 2009)
191932017-01-183384
36 Continuing Review & Changes of Protocol
192292017-01-187881
37 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-188542
38 Belmont Report
192002017-01-0638631
39 IRB Member Newsletter--Volume 5 (Spring/Summer 2012)
246302017-01-054314
40 How to Conduct a Modification Response Review in ARROW
206932017-01-045043

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