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No.Document TitleIDUpdatedHits
1 Belmont Report
192002017-01-0637994
2 Noncompliance, Protocol Exceptions and Deviations
192352018-01-2333423
3 For IRB Members
191192020-06-0229700
4 Unanticipated Problems and Serious Adverse Events
192432016-12-2717610
5 Genetic Testing or Analysis
197702017-11-2716230
6 Prisoners: Regulations
192402016-12-2710558
7 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-188377
8 Continuing Review & Changes of Protocol
192292017-01-187637
9 Informed Consent Process, Elements, and Waivers
192312017-07-147588
10 Privacy & Confidentiality
192372019-08-057581
11 Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications
217712017-03-277576
12 Drugs, Biologics, and Devices: Regulations
192412017-07-287341
13 Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance
192322019-03-077077
14 Primary Reviewer Guidance for Initial Reviews
196832017-03-277020
15 Reviewing IRB Meeting Minutes in ARROW
192272016-01-196099
16 Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
192282017-01-235857
17 How to Conduct PRS Review
205772017-08-185844
18 Brief Responsibilities of an MR-IRB Member
192062020-06-025820
19 Meeting Workspace Navigation Guide for IRB Members
205872016-12-195791
20 Finding Study-Related Documents in ARROW
192142017-01-235637

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