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    Business Continuity Planning for [Computer Systems] Operations

    View: 130

    Website https://www.compliance4all.com/control/w_product/~product_id=502164LIVE?channel=ourglocal_Nov_2018_S | Want to Edit it Edit Freely

    Category Disaster Recovery Planning, Computer Systems, FDA checklist, business continuity plan sample, FDA compliance requirements, Clinical Data Managers, Validation Specialists

    Deadline: November 07, 2018 | Date: November 09, 2018

    Venue/Country: Online, U.S.A

    Updated: 2018-09-07 15:31:59 (GMT+9)

    Call For Papers - CFP

    Overview:

    Computer system validation has been regulated by FDA for more than 30 years, as it relates to systems used in the manufacture, testing, distribution and management of a product in the pharmaceutical, biotechnology, medical device, animal health, tobacco and other regulated industries.

    Why should you Attend:

    The attendee will also learn how to develop a standard approach to planning, executing and documenting efforts that involve recovery of day-to-day business operations and data in a manner that complies with FDA guidelines. Some people may be new to the concept of validation and FDA regulation, and will have to be coached on how to follow any necessary procedures required for compliance.

    Areas Covered in the Session:

    Gain an understanding of disaster recovery and business continuity planning

    Develop the ability to apply FDA compliance requirements when developing a disaster recovery and business continuity plan

    Understand the best practices for developing a disaster recovery and business continuity plan

    Who Will Benefit:

    Information Technology Analysts

    QC/QA Managers and Analysts

    Clinical Data Managers and Scientists

    Compliance Managers

    Lab Analysts and Managers

    Computer System Validation Specialists

    Speaker Profile:

    Carolyn (McKillop) 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.