Search result for "": 41-60

No.	Document Title	ID	Updated	Hits
41	Unanticipated Problems and Serious Adverse Events	19243	2016-12-27	17739
42	Review Processes Other Than Full-Board	19242	2016-12-27	4852
43	Drugs, Biologics, and Devices: Regulations	19241	2017-07-28	7464
44	Prisoners: Regulations	19240	2016-12-27	10615
45	Pregnant Women, Fetuses and Neonates: Regulations	19239	2017-11-28	5616
46	Children as research participants: Regulations	19238	2018-12-04	4220
47	Privacy & Confidentiality	19237	2019-08-05	7725
48	Overview of the Accreditation Process and UW-Madison's Human Research Protections Program	19236	2017-02-15	5614
49	Noncompliance, Protocol Exceptions and Deviations	19235	2018-01-23	33628
50	Study Personnel Financial Conflicts of Interest and HS IRBs Review Guidance	19232	2019-03-07	7157
51	Informed Consent Process, Elements, and Waivers	19231	2017-07-14	7681
52	Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)	19230	2017-01-18	8457
53	Continuing Review & Changes of Protocol	19229	2017-01-18	7739
54	Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities	19228	2017-01-23	5937
55	Reviewing IRB Meeting Minutes in ARROW	19227	2016-01-19	6186
56	Initial Review Tips for IRB Members	19226	2018-03-19	4410
57	Cheat Sheet (w/ screenshots) for Initial Reviews in ARROW	19216	2017-01-23	4318
58	Finding Study-Related Documents in ARROW	19214	2017-01-23	5692
59	Reviewing Initial Applications In ARROW	19213	2017-08-07	3993
60	Brief Responsibilities of an MR-IRB Member	19206	2020-06-02	5901

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