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
Email: [email protected]