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    THIS GAMP® 5 TRAINING/WEBINAR WILL DISCUSS ON THE 2015 - GAMP® 5 as applied to FDA software validation - strategies to avoid warning letters

    View: 220

    Website http://bit.ly/1GVLtb8 | Want to Edit it Edit Freely

    Category Food,Drug

    Deadline: January 21, 2015 | Date: January 21, 2015

    Venue/Country: 2600 E. Bayshore Road, U.S.A

    Updated: 2014-12-19 04:36:44 (GMT+9)

    Call For Papers - CFP

    This GAMP® 5 training/Webinar will discuss on the GAMP® software validation model and the defined process of GAMP® 5 as it applied to FDA software validation.

    Why Should You Attend:

    Many companies struggle with understanding what FDA, MHRA, EU and other Ministries of Health want to see regarding software validation.This presentation will review the FDA validation process, the GAMP® software validation model, and the process defined in GAMP® 5 as it applies to FDA software validation. The attendee should leave the presentation confident in their ability to understand and apply the GAMP® 5 process.

    FDA inspectors are now being trained to evaluate software validation practices.

    Increasing use of automated manufacturing and quality systems means increased exposure

    Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny

    Corporate uncertainty leads to inaction and 'wheel spinning'

    A third of recent warning letters included citations with respect to improper or ineffective validation

    Areas Covered in the Webinar:

    Outline of FDA regulations as applied to software.

    Review of FDA software validation requirements.

    Why validation makes good business sense.

    Strategies on how to avoid the most common problems.

    The GAMP® approach.

    Advice on successful validation project staffing.

    GAMP® 5 Principles.

    GAMP® 5 as applied to FDDA software validation.

    Using GAMP® 5 to cut validation costs.

    Who Will Benefit:

    This seminar will give valuable help to FDA regulated Pharmaceutical, Medical Device, Biotech, Diagnostics and Biological manufacturers. The staff members who will benefit include:

    System owners - responsible for keeping individual systems in validation

    Policy makers fof software validation and software quality

    Software development life cycle (SDLC) personnel

    QA / QC managers, executives and personnel

    IT / IS managers and personnel

    Validation specialists

    Software quality reviewers

    Consultants

    For Registration:http://www.complianceonline.com/gamp-5-as-applied-to-fda-software-validation-strategies-to-avoid-warning-letters-webinar-training-701484-prdw?channel=Organic_Referral


    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.