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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20240329T142532Z
UID:d0980412-dae6-4b3f-aa0d-6cefdc1fa575
DTSTART:20210607T100000
DTEND:20210608T100000
CLASS:PRIVATE
DESCRIPTION:Overview:
\nThis webinar serves will provide substantive t
raining of the criteria
\nfor IRB approval for new IRB members/staff
who have less than
\nthree years of experience.
\n
\nWhy sh
ould you Attend:
\nWhat criteria should be applied to the review of s
tudies? When do
\nevaluations or quality assurance efforts require IR
B approval? How
\ncan an IRB appropriately protect vulnerable subject
s in research?
\nTo what degree should risks be minimized in research
studies? \;
\n
\nAreas Covered in the Session:
\nAppli
cability of HHS and FDA regulations for the protection of
\nhuman sub
jects
\nImportant definitions every IRB administrator/member must kno
w
\nHow to identify and minimize potential risks in a research study<
br />\nIRB'\;s role to determine that risks are reasonable in relation
to
\nanticipated benefits
\nIRB'\;s review of protocols to en
sure equitable selection of subjects
\n
\nWho Will Benefit:
\nIRB Members
\nIRB Administrators
\nIRB Managers
\n
\nSpeaker Profile:
\nGeorge Gasparis has over 35 years of experience
in the
\nadministration or conduct of human subjects research. Prior
to
\nfounding &ldquo\;PEER&rdquo\;\, he served as the Asst. VP and Sr
. Asst. Dean for
\nResearch Ethics at Columbia University (CU)\, CU M
edical Center
\n(CUMC) from 2003-12\, where he directed the IRB Offic
e and
\ncompliance team.
\n
\nEvent Fee: One Dial-in One At
tendee Price: US$150.00
\n
\nContact Detail:
\nCompliance4A
ll DBA NetZealous\,
\nPhone: +1-800-447-9407
\nEmail: support@co
mpliance4All.com
SUMMARY:Essential Training for IRB Members and Staff
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SUMMARY:Essential Training for IRB Members and Staff
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