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    FDA Regulations for Qualification and Validation Processes - 2017

    View: 134

    Website http://www.compliance4all.com/control/w_product/~product_id=501119LIVE?channel=mailer&camp=Webinar&A | Want to Edit it Edit Freely

    Category FDA Regulations, to be in compliance with regulatory trainings, medical devices to be in compliance, Qualifications, gamp 5, laboratory manager, clinical laboratory management, quality assurance, fda quality management system, FDA Compliance Training

    Deadline: April 27, 2017 | Date: April 28, 2017

    Venue/Country: Fremont, U.S.A

    Updated: 2017-02-24 19:09:27 (GMT+9)

    Call For Papers - CFP

    Overview:

    In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient.

    Why Should You Attend:

    The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for analytical equipment qualification and validation in your facility?

    Areas Covered in the Session:

    Requirements and approaches for Analytical Instrument Qualification

    Risk based validation approach

    Going through the qualification phases

    User requirements, writing the specifications

    Who Will Benefit:

    Laboratory managers, supervisors and analysts

    IT managers and staff

    Consultants

    Laboratory suppliers of material, equipment and services

    Senior quality managers

    Speaker Profile:

    Joy McElroy Upon earning a degree in Zoology at North Carolina State University, Joy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing Environmental Monitoring and Sterility Testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their Quality Control Lab.

    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.