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    Controlled Document System for a Life Sciences manufacturing plant - principles of Lean Documents and Lean Configuration - Webinar by GlobalCompliancePanel

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    Website http://bit.ly/17ZDlbr | Want to Edit it Edit Freely

    Category Webinar, Health, Medical, Pharma, Clinical

    Deadline: October 23, 2013 | Date: October 23, 2013

    Venue/Country: USA, U.S.A

    Updated: 2013-09-16 13:58:46 (GMT+9)

    Call For Papers - CFP

    Overview: Controlled documents are one of the foundational building blocks of a Quality Management System (QMS) for regulated industries. Too often, controlled documents are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed.

    This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to this key part of a QMS.

    Why you should attend: Do you find yourself constantly struggling to create, manage, and maintain all of the information found in controlled documents - which is often redundant, repetitive, and chained together in a cumbersome way? Do you find that your design and manufacturing resources are spending way too much time on documentation and not enough on engineering, quality, and operations? This webinar presents a fresh new approach based upon solid principles and proven practices - as well as an alternative that avoids many of the pitfalls of traditional ways of preparing these documents.

    Areas Covered In the Session:

    Brief introduction to Lean Documents and Lean Configuration

    Quality System Regulation, 21 CFR Part 820, and ISO 13485 as these apply to controlled documents.

    Typical controlled documents and functions

    Lean principles applied to controlled documents

    Lean principles applied to configuration of electronic QMS software

    Who will benefit:

    Managers, Supervisors, Directors, and Vice-Presidents in the areas of:

    R&D

    Manufacturing Engineering

    Quality Assurance

    Operations

    Document Control

    José Mora is a Principal Consultant specializing in Manufacturing Engineering and Quality Systems. For over 29 years he has worked in the medical device industry specializing in manufacturing, process development, tooling, and quality systems.

    NetZealous LLC,

    DBA GlobalCompliancePanel

    161 Mission Falls Lane,

    Suite 216, Fremont, CA 94539, USA

    USA Phone:800-447-9407

    Fax: 302-288-6884

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Event Link - http://bit.ly/17ZDlbr

    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.