Results: 41-60 of 65
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No.Document TitleIDUpdatedHits
41 Unanticipated Problems and Serious Adverse Events
192432016-12-2717739
42 Review Processes Other Than Full-Board
192422016-12-274852
43 Drugs, Biologics, and Devices: Regulations
192412017-07-287464
44 Prisoners: Regulations
192402016-12-2710615
45 Pregnant Women, Fetuses and Neonates: Regulations
192392017-11-285616
46 Children as research participants: Regulations
192382018-12-044220
47 Privacy & Confidentiality
192372019-08-057725
48 Overview of the Accreditation Process and UW-Madison's Human Research Protections Program
192362017-02-155614
49 Noncompliance, Protocol Exceptions and Deviations
192352018-01-2333628
50 Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance
192322019-03-077157
51 Informed Consent Process, Elements, and Waivers
192312017-07-147681
52 Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)
192302017-01-188457
53 Continuing Review & Changes of Protocol
192292017-01-187739
54 Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities
192282017-01-235937
55 Reviewing IRB Meeting Minutes in ARROW
192272016-01-196186
56 Initial Review Tips for IRB Members
192262018-03-194410
57 Cheat Sheet (w/ screenshots) for Initial Reviews in ARROW
192162017-01-234318
58 Finding Study-Related Documents in ARROW
192142017-01-235692
59 Reviewing Initial Applications In ARROW
192132017-08-073993
60 Brief Responsibilities of an MR-IRB Member
192062020-06-025901

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