Ended: Sept. 26, 2019
Sponsored by the MGH Division of Clinical Research, the Partners Human Research Office (IRB) and the Partners Human Research Quality Improvement Program (QI).
Speakers: Jo O'Driscoll-Davis, Assistant Director for Continuing Review and Administrative Chair Michael Ducey, Senior Human Resource Specialist and the Administrative Chair for BWH Panel B
Learn how your Continuing Review and Amendments are handled by the IRB staff at intake and what is required at full board for review. Also, how and what the Administrative Chairs (voting members of the IRB) review and consider at Continuing Review. The Administrative Chairs will use the PHRC Guide to Review of Non-Exempt Human Subjects Research to identify and discuss ethical and scientific issues, including how recruitment, consenting and safety monitoring is handled and how some of these issues can be addressed in your submission. This session is limited to 25 participants to facilitate interaction. Registration is required. Please contact Tiereny Morrison-Rohlfs at tmorrison-rohlfs@partners.org with any questions
Programs: Clinical Research Investigator Beginner Clinical Research Coordinator Experienced Clinical Research Coordinator
Categories: Clinical Research Ethical Oversight IRB
Sponsor: MGH Division of Clinical Research
Sessions
Sept. 26, 2019
09/26/19 12PM-1PM |
12 PM – 1 PM |
Garrod/Mendel, Floor 2, Simches Research Center
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Other Offerings
Past Offerings | |
---|---|
IRB Roundtable: Continuing Review and Amendments |
Nov. 1, 2018
11/1/18 |
IRB Roundtable: Continuing Review and Amendments |
Oct. 12, 2017
10/12/17 |
IRB Roundtable: Continuing Review and Amendments |
Oct. 13, 2016
10/13/16 |
Reviews
Date Reviewed: Sept. 26, 2019, 1:12 p.m.
Date Reviewed: Nov. 1, 2018, 3:20 p.m.
Date Reviewed: Nov. 1, 2018, 2:29 p.m.