Date :
Place : United States, New hyde park
Contact Person:atozcompliance
Description:
Learning FDA’s 21 CFR Part 11 compliance guidance on electronic records/electronic signatures (ER/ES) for computer systems is critical in developing the appropriate validation strategy for achieving the thoroughness required to prove that a system does what it purports to do, from conception through retirement.Deadline for abstracts/proposals : 17th February 2016
Organized By :atozcompliance
Keynote Speakers : Carolyn Troiano Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated industries. She is currently an independent consultant, advising companies on computer system validation and large-scale IT system implementation projects. During her career, Carolyn worked directly, or on a consulting basis, for many of the larger pharmaceutical companies in the US and Europe. She developed v
Conference Highlights :Overview This webinar will help you understand in detail the application of FDA’s 21 CFR Part 11 compliance guidance on electronic records/electronic signatures (ER/ES) for computer systems subject to FDA regulations. This is critical in order to develop the appropriate validation strategy and achieve the thoroughness required to prove that a system does what it purports to do. It also ensures that a system is maintained in a validated state throughout its entire life cycle, from conception
Venue :AtoZ Compliance 2754 80th Avenue, New Hyde Park, NY 11040
Check the event website for more details.