Date :
Place : United States, San Jose
Contact Person:Ashutos Swain
Description:
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. 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.Deadline for abstracts/proposals : 29th May 2021
Organized By :Complianceonline
Keynote Speakers :
Check the event website for more details.