Date :
Place : United States, Aurora
Website :https://bit.ly/3fqLhJA
Contact Person:Training doyens
Description:
Know about the 21 CFR Part 11 regulations on Electronic Records/Electronic Signatures and how to meet the compliance requirements. The webinar provides a condensed overview of the regulations and techniques to maintain compliance.Deadline for abstracts/proposals : 14th July 2020
Organized By :Training Doyens
Keynote Speakers : Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health and other FDA-regulated industries. She is currently managing a large, complex data migration, analytics and reporting program at a major financial institution.
Conference Highlights :OVERVIEW The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11 regulations. This includes development of a company philosophy and approach, and incorporating it into the overall computer system validation program and plans for individual systems that have this capability. FDA 21 CFR Part 11 was enacted in the late 1990s and implementation success across t
Venue :Training Doyens, East Walker Drive, Aurora, CO, USA
Check the event website for more details.