Verification vs Validation-Product, Process or Equipment and QMS Software

If you are unable to see the message below, [click here to view](. [Compliance4all] Knowledge. Creativity. Performance Live Webinar Verification vs Validation-Product, Process or Equipment and QMS Software Wednesday, February 05 2020 Time: 10:00 AM PST | 01:00 PM EST Duration: 90 Minutes [Register]( The verification and validation of regulated software is coming under increased scruinty by the U.S. FDA.This webinar will address the use of the FDA, GAMP, 21 CFR Part 11,"Electronic Records"/"Electronic Signatures", IEC 62304, and other applicable industry software validation models, coupled with the ISO 14971/ICH Q9 Product Risk Management models, to plan, structure, run, and document acceptable software validations. Speaker Profile John E. Lincoln, is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide. [Register]( Compliance4all NetZealous LLC, 39658 Mission Boulevard, Fremont, CA 94539, USA. [www.compliance4all.com]( Toll Free : +1-800-447-9407 If you do not wish to receive this training alerts from Compliance4All Click [Unsubscribe](