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Medical Device Verification & Validation

Harnessing Process Validation to Reduce Risk and Ensure Overall Product Quality

17-18 Jul 2019
Philadelphia, United States of America

Why You Should Attend

Medical Device Verification & Validation

Verification and validation remains to have a direct influence on the success of the product development effort. Ensuring quality engineering is critical in order to reduce risk to and establish processes in a more secure way. Those in the Life Sciences space are continuously looking for improvements to reduce cost, product timelines, and mistakes for overall better product success.

This premier marcus evans event will bring together the foremost leaders within the verification and validation space to identify methods and strategies for overall greater testing outcomes and risk management activities to ensure optimal product quality assurance.

Key Topics

  • Integrate risk management with V&V for greater product safety
  • Implement a sturdy VMP to assure product quality
  • Leverage different tools and technologies for improved process validation activities
  • Incorporate earlier processes in order to promote cost reduction, fewer errors, and faster market time
  • Interpret changes to the EU MDR in order to ensure optimal compliance

  • Why Choose marcus evans?

    marcus evans specialises in the research and development of strategic events for senior business executives. From our international network of 63 offices, marcus evans produces over 1000 event days a year on strategic issues in corporate finance, telecommunications, technology, health, transportation, capital markets, human resources and business improvement.

    Above all, marcus evans provides clients with business information and knowledge which enables them to sustain a valuable competitive advantage and makes a positive contribution to their success.

    Practical Insights From

    Miklos Szoke
    Verification & Validation Program Manager
    GE Healthcare

    Grant Short
    Medtronic Technical Fellow
    Medtronic Spine and Biologics

    Nishi Shah
    Verification Lead
    Baxter Healthcare

    Matthew Dittler
    Senior Quality Engineer
    Johnson and Johnson

    Kelly Lorenz, MBA, PMP
    Staff Quality Engineer, Corporate Validation Network Lead
    Becton Dickinson

    Mihir Vashi
    Validation Lead

    Bill Brodbeck, Ph.D
    Senior Director, Regulatory Affairs
    STERIS Corporation

    Jayet Moon
    Sr. Quality Engineer
    Terumo Medical Corporation

    Click Here For Full Agenda

    Voice of Our Customers
    • “This is a very informative conference; this was well organized – credit goes to the organizers.” Alcon Novartis
    • “Overall great use of two days. I learned many nuanced points on topics I already felt I had a good handle on. New information!” Medtronic
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    Event Contact

    For all enquiries regarding speaking, sponsoring and attending this conference contact:

    Melini Hadjitheori

    PO Box 24797
    CY-1304 Nicosia

    +357 22 849 308
    Fax: +357 22 849 394