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    Online Webinar :Creating and Maintaining a GMP Quality System

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    Website http://c2gowebinars.com/product/?topic=creating-and-maintaining-a-gmp-quality-system | Want to Edit it Edit Freely

    Category

    Deadline: August 04, 2016 | Date: August 04, 2016

    Venue/Country: Online, U.S.A

    Updated: 2016-06-09 16:46:29 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    Creating and Maintaining a GMP Quality System

    Why should you attend :

    If you are a quality assurance or quality control professional working at a Pharma, medical device or biotech company, the FDA requires you to implement a GMP compliant system, this webinar will give you a basic roadmap.

    Areas Covered in the Session:

    What is a GMP compliant quality system, elements of quality system,21 CFR Parts 210/211 requirements, the quality unit, SOPs and documentation, how to create a quality system.

    Who will benefit: (Titles)

    Quality control professionals

    Quality assurance professionals

    Operations and management in a FDA regulated environment

    Webinar includes:

    Q/A Session with the Expert to ask your question

    PDF print only copy of PowerPoint slides

    60 Minutes Live Presentation

    Certificate of attendance

    For Registration :http://c2gowebinars.com/product/?topic=creating-and-maintaining-a-gmp-quality-system

    Note: Use coupon code    and get 15% off on registration.


    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.