Essential Training for IRB Members and Staff
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Training by
Compliance4All
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On-Site
/ Training
USD 150.00
Details
Overview:
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
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
Outline
Speaker/s
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.
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.
Special Offer
One Dial-in One Attendee
Price: $150.00
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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 has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.
Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.
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