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Essential Training for IRB Members and Staff
Presented By Netzealous LLC DBA - Compliance4All
Tuesday, June 5th at 10:00am PST
Online sale ends: 06/04/18 at 9:00am PST
Online
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539
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Talent
Description
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 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: support@compliance4All.com |
Presented By
10:00am to 11:30am
General Admission: $150.00
All Ages
50 18004479407 UPCOMING EVENTS
PAST EVENTS
Friday, April 20th
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