Date :
Place : United States, Fremont
Contact Person:Event Manager
Description:
Overview: 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. Why should you Attend: This webinar will help you understand in detail the application of FDA's 21 CFR Part 11 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.Deadline for abstracts/proposals : 20th June 2018
Organized By :Compliance4All DBA NetZealous
Keynote Speakers :
Venue :Fremont, CA, USA
Check the event website for more details.