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No.Document TitleIDUpdatedHits
1 Belmont Report
192002017-01-0638694
2 Noncompliance, Protocol Exceptions and Deviations
192352018-01-2333922
3 For IRB Members
191192020-06-0230179
4 Unanticipated Problems and Serious Adverse Events
192432016-12-2717902
5 Genetic Testing or Analysis
197702017-11-2716643
6 Prisoners: Regulations
192402016-12-2710683
7 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-188555
8 Continuing Review & Changes of Protocol
192292017-01-187899
9 Privacy & Confidentiality
192372019-08-057858
10 Informed Consent Process, Elements, and Waivers
192312017-07-147834
11 Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications
217712017-03-277739
12 Drugs, Biologics, and Devices: Regulations
192412017-07-287574
13 Primary Reviewer Guidance for Initial Reviews
196832017-03-277234
14 Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance
192322019-03-077229
15 Reviewing IRB Meeting Minutes in ARROW
192272016-01-196267
16 Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
192282017-01-236024
17 How to Conduct PRS Review
205772017-08-186000
18 Brief Responsibilities of an MR-IRB Member
192062020-06-025982
19 Meeting Workspace Navigation Guide for IRB Members
205872016-12-195943
20 Finding Study-Related Documents in ARROW
192142017-01-235772

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