Search result for "": 21-40

No.	Document Title	ID	Updated	Hits
21	Making a Motion at IRB Meetings	31523	2017-08-11	4556
22	Reviewing Initial Applications In ARROW	19213	2017-08-07	4075
23	Drugs, Biologics, and Devices: Regulations	19241	2017-07-28	7566
24	Informed Consent Process, Elements, and Waivers	19231	2017-07-14	7822
25	New IRB Members Guide	24684	2017-05-22	4868
26	IRB Member Newsletter--Volume 8 (Winter 2013)	36105	2017-04-18	4348
27	IRB Member Newsletter--Volume 7 (Spring 2013)	29747	2017-04-18	3942
28	Primary Reviewer Guidance for Initial Reviews	19683	2017-03-27	7220
29	Guidance for UW Madison Health Sciences IRB & Minimal Risk IRB Primary Reviewers for Summarizing Initial Review Applications	21771	2017-03-27	7728
30	Overview of the Accreditation Process and UW-Madison's Human Research Protections Program	19236	2017-02-15	5668
31	IRB Member Newsletter--Volume 2 (Winter 2010)	19194	2017-01-30	3459
32	Finding Study-Related Documents in ARROW	19214	2017-01-23	5766
33	Cheat Sheet (w/ screenshots) for Initial Reviews in ARROW	19216	2017-01-23	4362
34	Brief Overview of Regulatory Basis of IRB Authority and Review Responsibilities	19228	2017-01-23	6013
35	IRB Member Newsletter--Volume 1 (Fall 2009)	19193	2017-01-18	3384
36	Continuing Review & Changes of Protocol	19229	2017-01-18	7881
37	Criteria for IRB Approval: 45 CFR 46.111 (DHHS), 21 CFR 56.111 (FDA), and 38 CFR 16.111 (VA)	19230	2017-01-18	8542
38	Belmont Report	19200	2017-01-06	38631
39	IRB Member Newsletter--Volume 5 (Spring/Summer 2012)	24630	2017-01-05	4314
40	How to Conduct a Modification Response Review in ARROW	20693	2017-01-04	5043

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