Results: 21-40 of 66
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No.Document TitleIDUpdatedHits
21 Children as research participants: Regulations
192382018-12-044356
22 Continuing Review & Changes of Protocol
192292017-01-187980
23 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-188628
24 Drugs, Biologics, and Devices: Regulations
192412017-07-287657
25 Finding Study-Related Documents in ARROW
192142017-01-235859
26 For IRB Members
191192021-03-0930402
27 Genetic Testing or Analysis
197702017-11-2716803
28 Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications
217712017-03-277821
29 How to Conduct a Deferral Response Review in ARROW
206942016-12-195126
30 How to Conduct a Modification Response Review in ARROW
206932017-01-045123
31 How to Conduct PRS Review
205772017-08-186066
32 IEP IRB Member FAQ
1095872021-03-0965
33 Informed Consent Process, Elements, and Waivers
192312017-07-147956
34 Initial Review Tips for IRB Members
192262018-03-194535
35 IRB Member FAQs
246852020-06-025138
36 IRB Member Newsletter -- Volume 12 (Summer 2019)
923632019-06-121014
37 IRB Member Newsletter--Scheduling Special Edition
770202018-04-111986
38 IRB Member Newsletter--Volume 1 (Fall 2009)
191932017-01-183436
39 IRB Member Newsletter--Volume 10 (Fall 2017)
764652017-09-122529
40 IRB Member Newsletter--Volume 11 (Spring 2018)
812332019-06-121884

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