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2-Hour Virtual Seminar on The 6 Most Common Problems in FDA Software Validation and Verification

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compliance4all.com

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info@mail.compliance4all.com

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Wed, Oct 30, 2019 03:12 PM

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If you are unable to see the message below, . This webinar describes the validation planning process

If you are unable to see the message below, [click here to view](. [Compliance4all] Knowledge. Creativity. Performance Live Webinar 2-Hour Virtual Seminar on The 6 Most Common Problems in FDA Software Validation and Verification Thursday, November 07 2019 Time: 10:00 AM PST | 01:00 PM EST Duration: 2 Hours [Register]( This webinar describes the validation planning process with particular emphasis on avoiding six common pitfalls. Increased use of software from automated manufacturing and quality systems means increased exposure. Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny. Speaker Profile David Nettleton , is an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation. His latest book is "Risk Based Software Validation - Ten easy Steps" that relates to the development, purchase, installation, operation and maintenance of computerized systems used in regulated applications. [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](

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