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8th Medical Device Safety Monitoring & Reporting

Optimizing Device Monitoring Process to Increase Overall Patient Safety While Overcoming Security and Reporting Hurdles

28-30 Jan 2020
San Diego, CA, United States of America


Why You Should Attend

8th Medical Device Safety Monitoring & Reporting

Attending this 8th marcus evans event will allow attendees the opportunity to broaden and strengthen their safety measures while streamlining measures to maintain and meet regulatory sanctions.

The Medical Device arena is constantly updating methods to best conduct device monitoring and reporting, it is imperative for companies to continually amend practices in order to maintain compliance, optimize device safety and maintain a competitive edge. With EU MDR compliance deadlines around the corner, this is a critical time for companies to identify and crowd check plans for meeting regulations. Additionally, in a world where technology is king, Medical Device manufacturers continue to find new ways to incorporate tech in the device realm, creating a more significant and diverse measure of safety than ever before. 

 

Key Topics

  • Bolster remainder of transition period with EU MDR by benchmarking best practices for implementation
  • Enhance reporting procedures to meet global regulatory systems
  • Strengthen patient safety and security through improved cybersecurity practices
  • Streamline Periodic Safety Update Reports (PSUR) through enhanced understanding of expectations
  • Conduct postmarket surveillance and monitoring through digital media auditing to determine and leverage real world data

  • 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

    Pearley Bhambri
    VP, QA - Global Quality Systems and Compliance
    Hill-Rom

    David Scott
    Associate Director, Medication Management Solutions
    BD

    Gerwin de Graaff
    Sr. Director Global Vigilance | Quality
    Medtronic

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

    Joseph Purpura
    Associate Vice President, Medical Device Safety - Global Patient Safety & Epidemiology
    Allergan

    Gia Rozells
    Director, User Experience Design
    Becton Dickinson

    Michelle Hughes
    Director QA - Vigilance & Complaint Systems
    ResMed

    Malik Khan
    Director of Quality Assurance
    Stryker

    Click Here For Full Agenda

    Voice of Our Customers
    • “A good mix of participants with valuable perspectives to share.” – Baxter International
    • “One of the best conferences since all the topics covered were relevant and timely while providing a great atmosphere for networking.” – Endologix
    • “I am new to the medical device industry. This conference was very informative and helpful for me. All the speakers were excellent and knowledgeable.” – Edwards Lifesciences
    • “Very good & broad overview of MDR process and emerging issues. Great reference material for internal training.” – Abbott Diabetes
    • ”Great interactive event and learning on topics related to medical devices, challenges and solutions. Also great for networking.” – St. Jude Medical
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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


    Telephone:
    +1 312 540 6347
    Fax: +1 312 276 8505
    Email: MeliniH@marcusevansch.com