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9th Medical Device Safety Monitoring and Reporting

Sustaining Long Term Quality Through Enhanced Device Surveillance While Exceeding Compliance

3-4 Feb 2021
An Online and Fully Engaged Event, United States of America

Why You Should Attend

9th Medical Device Safety Monitoring and Reporting

Medical device companies continue to look at new strategies, tools, and technologies to achieve a more comprehensive medical device monitoring and reporting framework to ensure highest quality and safety of products. This 9th installment of the Medical Device Safety Monitoring and Reporting Conference will bring together leading professionals in regulatory affairs, compliance, post market surveillance, complaint handling, and in other related roles to address emerging compliance concerns, risk management trends, and product safety measures through a more integrated approach to monitoring and reporting.

Our interactive and fully engaging platform enables high levels of participation with AI Powered Matchmaking, 1:1 Meetings, Schedule Customization, Breakout Rooms, Live Polling, Surveys, Games, Quizzes and More! You control your connections with your industry peers and the content you want in a flexible and efficient format!

Key Topics

  • Look to the future of surveillance and reporting through the scope of Covid-19
  • Monitor Device Post Market through Literature Reviews
  • Create Practices for IVDR in Preparation for Current May 2022 Deadline
  • Enhance Investigations Conducted with Complaints to Streamline Methods for Conducting Root Cause Analysis
  • Capitalize on long-term quality through streamlined surveillance

  • 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

    Christina Arnt
    Post Market Surveillance Director
    Zimmer Biomet

    Sylvie Bartus
    Director, Safety Officer, Global Clinical Affairs
    Edwards Lifesciences

    Michael Hopkinson
    QA Leader
    GE Healthcare

    Maria Zollini
    Customer Quality Engineer

    Michael Drues
    Vascular Sciences

    Sharon Perez
    Director, Global Medical Device Safety

    Wendel Smith
    VP Product Safety Quality-Global Quality
    Edwards Life Sciences

    Eric Henry
    Senior Quality & Regulatory Compliance Advisor, FDA & Life Sciences Practice
    King & Spalding

    Click Here For Full Agenda

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    Event Contact

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

    Melini Hadjitheori

    455 N Cityfront Plaza 9th Floor,
    Chicago, 60611, USA

    +1 312 540 6347
    Fax: +1 312 276 8505