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    Master Validation Plan - A Complete Package

    View: 128

    Website http://www.onlinecompliancepanel.com/webinar/MASTER-VALIDATION-PLAN-501173/DEC-2015-ES-OURGLOCAL | Want to Edit it Edit Freely

    Category Validation,Equipment validation, VMP, Master Validation Plan

    Deadline: December 07, 2015 | Date: December 08, 2015

    Venue/Country: online Webinar, U.S.A

    Updated: 2015-11-25 19:00:00 (GMT+9)

    Call For Papers - CFP

    Master Validation Plan - A Complete Package

    Master Validation Plan

    Instructor: Marie Dorat

    Product ID: 501173

    Description

    This course will provide guidance on best practices for developing and implementing a good plan detailing responsibilities and deliverables to make validation efficient and consistent. It will provide a step-by-step guidance for medical device companies that need to develop a validation master plan (VMP) for product/equipment transfer, facilities, processes or to develop a company standard.

    Objectives of the Presentation

    What is a VMP and how is it valuable to my company?

    What topics are covered in the VMP and to what extent?

    How is the VMP controlled and updated?

    How is the VMP implemented?

    Who contributes to the VMP?

    Why Should you Attend

    The Validation Master Plan webinar describes the way an organization may approach validation; help identify who controls the various aspects of the validation activities and how production, quality and management will be involved. The VMP also details the validation requirements for each test/ system/ equipment and will guide the organization in achieving its objectives.

    Areas Covered

    Overview of Validation Master Plan

    What is a VMP?

    Which regulations apply?

    What topics are covered in the VMP?

    Master Validation Plan content

    Purpose

    Scope

    Project approach

    Key activities

    Project organization

    Communication plan

    Quality assurance

    Who are the VMP Key contributors? Defining their roles

    Quality Assurance

    Regulatory Affairs

    Operations

    Engineering

    Implementation of the VMP

    Training requirements

    Controlling and updating the VMP

    Who can Benefit

    Medical device/IVD companies & Manufacturers

    Quality Assurance

    Quality Engineers

    QA Managers

    For Registration -

    http://www.onlinecompliancepanel.com/webinar/MASTER-VALIDATION-PLAN-501173/DEC-2015-ES-OURGLOCAL

    Note : Use coupon code 1371 and get 10% 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.