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    Best Practices to Support FDA Computer System Validation

    View: 108

    Website http://www.compliance4all.com/control/w_product/~product_id=502005LIVE?channel=ourglocal_Aug_2018_SE | Want to Edit it Edit Freely

    Category Computer System Validation, 21 cfr part 11 validation, computer system validation in pharmaceutical, fda 21 cfr part 11, computer system validation guidelines

    Deadline: August 05, 2018 | Date: August 07, 2018

    Venue/Country: Online, U.S.A

    Updated: 2018-06-07 14:30:17 (GMT+9)

    Call For Papers - CFP

    Overview:

    We will cover the importance of maintaining the documentation

    from every computer system validation effort in a "current" state.

    The system must be maintained in a validated state throughout its

    entire life cycle, and the accompanying validation documentation

    must also be maintained.

    Why should you Attend:

    This session will address the specific way of documenting your

    computer system validation work to ensure it meets FDA

    requirements and can pass an inspection. There are specific

    requirements that must be followed in order for the Agency to

    consider the documentation valid, and without following these,

    there is a great risk of invalidating work.

    Areas Covered in the Session:

    21 CFR Part 11, Electronic Records/Electronic Signatures (ER/ES)

    Data Archival to ensure security, integrity and compliance

    Learn the requirements for documenting efforts related to systems

    governed by FDA

    Discuss the best practices for documenting computer system

    validation efforts, including requirements, design, development,

    testing and operational maintenance procedures

    Who Will Benefit:

    Information Technology Analysts

    Information Technology Developers and Testers

    QC/QA Managers and Analysts

    Analytical Chemists

    Laboratory Managers

    Automation Analysts

    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.
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