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. 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.

Date : 10th October 2017 to 10th October 2017

Place : United States, Fremont

Website :http://www.compliance4all.com/control/w_product/~product_id=501506LIVE?channel=allconferencealerts_Oct_2017_SEO

Contact Person:Event Manager

Description:

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. 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.

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. 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. will be held in Fremont,United States on date 2017-10-10

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Deadline for abstracts/proposals : 9th October 2017

Keynote Speakers :

Venue :Fremont, CA, United States

Check the event website for more details.