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Live Online Training for PECB ISO 13485 Lead Auditor Certification Exam

    Live Online Training for PECB ISO 13485 Lead Auditor Certification Exam

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    Smatica conducts multiple batches for PECB ISO 13485 Lead Auditor live online training, starting every Monday, in different time zones, as mentioned below:

    10 AM US Central Time
    9 AM Eastern European time
    8 AM United Kingdom
    10 AM Dubai UAE
    9 AM Saudi Arabia, Kuwait & Qatar
    9 AM Sydney Australia
    7 AM Fiji
    9 AM Singapore

    Why should you attend?

    ISO 13485 Lead Implementer training enables you to develop the necessary expertise to support an organization in establishing, implementing, managing and maintaining a Medical Devices Quality Management System (MDQMS) based on ISO 13485. During this training course, you will also gain a thorough understanding of the best practices of Medical Devices Quality Management Systems and be able to improve an organization`s overall performance by consistently providing safe and qualitative medical devices.

    After mastering all the necessary concepts of Medical Devices Quality Management Systems, you can sit for the exam and apply for a “PECB Certified ISO 13485 Lead Implementer” credential. By holding a PECB Lead Implementer Certificate, you will be able to demonstrate that you have the practical knowledge and professional capabilities to implement ISO 13485 in an organization.

    Who should attend?

    • Managers or consultants involved in Medical Devices Quality Management
    • Expert advisors seeking to master the implementation of a Medical Devices Quality Management System
    • Individuals responsible for maintaining conformance with MDQMS requirements
    • MDQMS team members

    Learning objectives

    • Acknowledge the correlation between ISO 13485 and other standards and regulatory frameworks
    • Master the concepts, approaches, methods and techniques used for the implementation and effective management of a MDQMS
    • Learn how to interpret the ISO 13485 requirements in the specific context of an organization
    • Learn how to support an organization to effectively plan, implement, manage, monitor and maintain a MDQMS
    • Acquire the expertise to advise an organization in implementing Medical Devices Quality Management System best practices

    Educational approach

    • This training is based on both theory and best practices used in the implementation of a MDQMS
    • Lecture sessions are illustrated with examples based on case studies
    • Practical exercises are based on a case study which includes role playing and discussions
    • Practice tests are similar to the Certification Exam

    Prerequisites

    A fundamental understanding of ISO 13485 and comprehensive knowledge of implementation principles.

    General Information

    • Certification and examination fees are included in the price of the training course
    • Training material containing over 450 pages of information and practical examples will be distributed
    • An attestation of course completion worth 31 CPD (Continuing Professional Development) credits will be issued to the participants who have attended the training course.
    • In case of exam failure, you can retake the exam within 12 months for free

    To register for this event please visit the following URL: https://www.smatica.com/product/iso-13485-lead-auditor/ →

     

    Date And Time

    07-11-2022 @ 10:00 AM to
    07-12-2022 @ 06:00 PM
     

    Registration End Date

    07-11-2022
     

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