Overview We will discuss the importance of applying industry best practices when validating laboratory systems that are regulated by FDA. Any GxP system (i.e., the system touches product during the laboratory testing or process) must be validated in accordance with FDA guidelines for computerized systems and documented accordingly. For more detail please click on this below link: http://bit.ly/2r9k1XA Email: [email protected] Toll Free: +1-844-746-4244 Tel: +1-516-900-5515 Fax: +1-516-900-5510

Date : 13th June 2017 to 13th June 2017

Place : United States, New york

Website :http://bit.ly/2r9k1XA

Contact Person:Compliance Global Inc.

Description:

Overview We will discuss the importance of applying industry best practices when validating laboratory systems that are regulated by FDA. Any “GxP” system (i.e., the system "touches" product during the laboratory testing or process) must be validated in accordance with FDA guidelines for computerized systems and documented accordingly. For more detail please click on this below link: http://bit.ly/2r9k1XA Email: [email protected] Toll Free: +1-844-746-4244 Tel: +1-516-900-5515 Fax: +1-516-900-5510

Overview We will discuss the importance of applying industry best practices when validating laboratory systems that are regulated by FDA. Any GxP system (i.e., the system touches product during the laboratory testing or process) must be validated in accordance with FDA guidelines for computerized systems and documented accordingly. For more detail please click on this below link: http://bit.ly/2r9k1XA Email: [email protected] Toll Free: +1-844-746-4244 Tel: +1-516-900-5515 Fax: +1-516-900-5510 will be held in New york,United States on date 2017-06-13

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Deadline for abstracts/proposals : 13th June 2017

Keynote Speakers :

Venue :2754 80th Avenue, New Hyde Park, NY 11040, United States

Check the event website for more details.