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    Integration of ERP and Legacy FDA 2017

    View: 132

    Website http://www.compliance4all.com/control/w_product/~product_id=501509LIVE?channel=ourglocal_Dec_2017_SE | Want to Edit it Edit Freely

    Category Laboratory Automation System, biotechnology, FDA guidelines, medical device calibration, fda quality management system, Technology Developers, science industries

    Deadline: December 04, 2017 | Date: December 05, 2017

    Venue/Country: Fremont, U.S.A

    Updated: 2017-10-31 15:46:18 (GMT+9)

    Call For Papers - CFP

    Overview:

    In this webinar speaker will discuss the best practices necessary to develop an integrated laboratory and business data collection, analysis and reporting computer system validation program.

    Why should you Attend:

    Those users accessing the business system must also not be able to enter or alter data directly into the laboratory system, unless it is clearly a requirement based on the process being followed.

    Areas Covered in the Session:

    Identify the key input and output points that will warrant greater scrutiny as the integrated system is tested and validated

    Discuss the steps for validating systems, along with the key documentation associated with maintaining the systems in a validated state, while minimizing costs

    Learn how to leverage these practices across all systems by creating a standardized program for integrating FDA-regulated and non-regulated systems

    Understand the additional training that must be provided to business and IT staff involved in the integration process

    Who Will Benefit:

    Clinical Data Managers and Scientists

    Analytical Chemists

    Laboratory Managers

    Automation Analysts

    Speaker Profile:

    Carolyn Troiano has more than 35 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs.

    Event Fee: One Dial-in One Attendee Price: US$150.00

    Contact Detail:

    Compliance4All DBA NetZealous,

    Phone: +1-800-447-9407

    Email: supportatcompliance4All.com


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.