Results : 21-40 of 66
XML   JSON  
Search result for "": 21-40
No.Document TitleIDUpdatedHits
21 How to Conduct PRS Review
205772017-08-187137
22 Making a Motion at IRB Meetings
315232017-08-115732
23 Reviewing Initial Applications In ARROW
192132017-08-074859
24 Drugs, Biologics, and Devices: Regulations
192412017-07-288636
25 Informed Consent Process, Elements, and Waivers
192312017-07-148960
26 New IRB Members Guide
246842017-05-225792
27 IRB Member Newsletter--Volume 8 (Winter 2013)
361052017-04-185193
28 IRB Member Newsletter--Volume 7 (Spring 2013)
297472017-04-184861
29 Primary Reviewer Guidance for Initial Reviews
196832017-03-278806
30 Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications
217712017-03-278913
31 Overview of the Accreditation Process and UW-Madison's Human Research Protections Program
192362017-02-156545
32 IRB Member Newsletter--Volume 2 (Winter 2010)
191942017-01-304101
33 Finding Study-Related Documents in ARROW
192142017-01-236973
34 Cheat Sheet (w/ screenshots) for Initial Reviews in ARROW
192162017-01-235245
35 Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
192282017-01-237185
36 IRB Member Newsletter--Volume 1 (Fall 2009)
191932017-01-184100
37 Continuing Review & Changes of Protocol
192292017-01-189214
38 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-189691
39 Belmont Report
192002017-01-0641816
40 IRB Member Newsletter--Volume 5 (Spring/Summer 2012)
246302017-01-055075

Previous  1  2  3  4  Next


Not finding what you are looking for? Suggest a new document be created.