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3rd Risk Based Quality Management for Medical Devices

Incorporate a robust yet agile risk based framework to proactively address global compliance standards and achieve highest product safety in meeting patient needs

19-20 Sep 2018
Minneapolis, MN, United States of America


Why You Should Attend

3rd Risk Based Quality Management for Medical Devices

This marcus evans conference will bring together quality, regulatory affairs, and compliance professionals to benchmark global quality management systems against other peer organizations, interpret the upcoming EU MDR guidance’s, as well as provide case studies in the successful implementation of the recent changes in ISO 13485 and 14971 standards.

To download the agenda, please click here.

Key Topics

  • Recognize the impact of forthcoming international regulations on the medical device industry in order to remain competitive
  • Foster a quality and risk-centric culture by adopting proven change management techniques
  • Cultivate a successful partnership to suppliers and contract manufacturers that have equivalent risk and quality standards
  • Establish a real time post market surveillance system that feeds into the comprehensive risk management strategy
  • Ensure audit preparedness through comprehensive training protocols and internal process reviews
  • Previous Attendees Include

    Penumbra Inc, Wipro Technologies, Draeger, Acclarent, Fresenius Medical Care, Elekta Limited, Novocure, Covidien Gi Solutions, Draeger, Coloplast Corp., Suneva Medical Inc., Bayer Healthcare, Halyard Health, Medtronic Inc., St. Jude Medical, GE Healthcare, Integra Lifesciences, Intuitive Surgical Inc, Zimmer Inc., Medtronic Neuromodulation, Cardinal Health, Merit Medical Systems, Edwards Lifesciences, McKesson Corporation, and many more!


    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.




    Event Partners


    Practical Insights From

    Darin Oppenheimer
    Executive Director, Head Drug Device Center of Excellence
    Merck

    Tom Bento
    Sr. VP of Quality & Regulatory Assurance
    Nihon Kohden America

    Chirag Tilara
    Sr. Director of Global Quality
    Medtronic

    Jim Frett
    Global QA Director
    GE Healthcare

    Malik Khan
    Director of Quality
    Stryker

    Ian G. Welsford, Ph.D.
    Chief Compliance Officer
    EOFlow Inc.

    Laura LeBoeuf
    VP Quality, Regulatory, Clinical
    Apollo Endosurgery, Inc.

    Joshua Levin
    Associate Director, Manufacturing Quality
    Personal Genome Diagnostics

    Click Here For Full Agenda

    Voice of Our Customers
    • “The conference was very informative due to the content presented and experience level and professionalism of those involved. Also, the interactive sessions allowed opportunity to better understand and drive beyond the content to a level where the participants could provide specific details of interest.” – Arthrex
    • “Excellent presentations on relevant topics made by knowledgeable professionals. Great location and networking opportunities as well. Very well done!” – LEO Pharma
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    Event Contact

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

    Amanda Pink


    NBC Tower, 9th Floor
    455 North Cityfront Plaza Drive, Chicago
    Chicago, IL 60611

    Telephone:
    312-540-3000 Ext: 6310
    Fax: 312-540-3000 Ext: 6327
    Email: amandap@marcusevansch.com