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No.Document TitleIDUpdatedHits
1 Belmont Report
192002017-01-0641815
2 Noncompliance, Protocol Exceptions and Deviations
192352018-01-2336283
3 For IRB Members
191192021-03-0932600
4 Unanticipated Problems and Serious Adverse Events
192432016-12-2720020
5 Genetic Testing or Analysis
197702017-11-2718516
6 Prisoners: Regulations
192402016-12-2711671
7 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-189691
8 Continuing Review & Changes of Protocol
192292017-01-189214
9 Informed Consent Process, Elements, and Waivers
192312017-07-148960
10 Privacy & Confidentiality
192372019-08-058939
11 Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications
217712017-03-278913
12 Primary Reviewer Guidance for Initial Reviews
196832017-03-278806
13 Drugs, Biologics, and Devices: Regulations
192412017-07-288636
14 Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance
192322019-03-078171
15 Reviewing IRB Meeting Minutes in ARROW
192272016-01-197268
16 Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
192282017-01-237185
17 How to Conduct PRS Review
205772017-08-187137
18 Brief Responsibilities of an MR-IRB Member
192062020-06-027050
19 Finding Study-Related Documents in ARROW
192142017-01-236973
20 Meeting Workspace Navigation Guide for IRB Members
205872016-12-196934

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