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Site language : English - Français
Ref : 26943
Event :Essential Training for IRB Members and Staff

Date :Tuesday June 05th, 2018

Location :Online (Internet, Videoconferencing, ...)

Type :Education - International audience

Accreditation :--


Further information

This webinar serves will provide substantive training of the criteria 
for IRB approval for new IRB members/staff who have less than 
three years of experience.
Why should you Attend:
What criteria should be applied to the review of studies? When do 
evaluations or quality assurance efforts require IRB approval? How 
can an IRB appropriately protect vulnerable subjects in research? To 
what degree should risks be minimized in research studies? 
Areas Covered in the Session:
Applicability of HHS and FDA regulations for the protection of 
human subjects
Important definitions every IRB administrator/member must know
How to identify and minimize potential risks in a research study
IRB's role to determine that risks are reasonable in relation to 
anticipated benefits
IRB's review of protocols to ensure equitable selection of subjects
Who Will Benefit:
IRB Members
IRB Administrators
IRB Managers
Speaker Profile:
George Gasparis has over 35 years of experience in the 
administration or conduct of human subjects research. Prior to 
founding “PEER”, he served as the Asst. VP and Sr. Asst. Dean for 
Research Ethics at Columbia University (CU), CU Medical Center 
(CUMC) from 2003-12, where he directed the IRB Office and 
compliance team.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407

Further information

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Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All [...]

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