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    Webinar On Building a Compliant Documentation and Training System

    View: 331

    Website https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1460 | Want to Edit it Edit Freely

    Category Food, Drugs & Biologics

    Deadline: January 26, 2015 | Date: January 26, 2015

    Venue/Country: Mississauga, Canada

    Updated: 2014-11-28 17:55:29 (GMT+9)

    Call For Papers - CFP

    This 60 minutes webinar will give a better understanding of the relationship between compliance, documentation, and training. It will provide participants with the ability to effectively meet regulatory requirements, properly integrate training into their quality system, and develop effective compliance documentation that meets both regulatory and training purposes.

    There is an increasing trend for regulatory agencies to view compliance documentation and training with increased scrutiny. Documentation and training that is improperly developed, implemented, and/or recorded presents a significant regulatory risk for manufacturers. In addition to meeting regulatory requirements, documentation and training, that is properly developed, also can serve as the basis for a well-controlled operation and a highly-competent workforce.

    Areas Covered in the Session :

    Global regulatory requirements for compliance documentation and training

    The relationship between compliance documentation and training

    Read and understand versus demonstrated competence

    Regulatory requirements

    Elements of a compliant documentation and training system

    How to conduct a compliance documentation and training analysis

    Compliance documentation and training as the basis for world-class operational control and performance improvement

    Who Will Benefit:

    A must attend webinar for all personnel / companies in the Pharmaceuticals, Medical Devices, Biotechnology, Cosmetics, Personal Products, Foods & Beverages fields. The professionals who will benefit include all:

    Training Managers and Directors

    Regulatory Affairs

    Quality Professionals

    Documentation department

    Compliance officer

    Product Development Professionals

    QA/QC analysts

    Internal Auditors

    Quality Assurance scientists

    Production

    Operations

    Consultants

    Quality Unit managers and supervisors

    Price Tags:

    Live

    Single Live : For One Participant

    $ 249

    Corporate Live : For Max. 10 Participants

    $ 899

    Recording

    Single REC : For One Participant - Unlimited Access for 6 Months

    $ 299

    For more information and enquiries contact us at

    Compliance Trainings

    5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada

    Customer Support : #416-915-4458

    Email : supportatcompliancetrainings.com

    For more information about this event please visit

    https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1460


    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.