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6th Annual Medical Device Safety Monitoring and Reporting

Fortifying Strategies for Proactive Device Safety through Comprehensive Post Market Surveillance While Maintaining Global Compliance

24-25 Jan 2018
Planet Hollywood Resort & Casino | Las Vegas, NV, United States of America


Why You Should Attend

6th Annual Medical Device Safety Monitoring and Reporting

This 6th 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.

 

Key Topics

  • Improve post market surveillance strategies through efficient and effective practice
  • Mitigate safety concerns through a proactive focus on risk assessments
  • Unpack new and forthcoming regulations and guidances to achieve global compliance
  • Reinforce importance and Advance strategies for cybersecurity
  • Upgrade reporting tactics to maintain and streamline compliance
  • Previous Attendees Include

    Abbott Diagnostics, Allergan, Baxter International, Becton Dickinson, bioMérieux, Boston Scientific, C.R. Bard Inc., Covidien Ltd., Edwards Lifesciences, Eli Lilly and Company, Endologix, GE Healthcare, HealthTronics Inc., Medtronic Inc., Smith & Nephew, Smiths Medical, St. Jude Medical Inc., Stryker Corporation, Thermo Fisher Scientific, Thoratec Corporation


    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

    Evan Jacobs
    Chief, Information Analysis Branch Division of Postmarket Surveillance CDRH
    FDA

    Michelle Rios, MS
    Chief, MDR Policy Branch Division of Postmarket Surveillance - CDRH
    FDA

    Joseph Purpura
    Executive Director, Medical Device Safety Physician Medical Devices Global Patient Safety & Epidemiology
    Allergan

    Laura Meyer
    Post Market Surveillance Lead/Quality Engineer
    Siemens Healthineers

    Jessica Lee, PhD
    Director of Quality
    Boston Scientific

    Caroline Leab
    Director Regulatory Affairs
    St. Jude Medical

    Angela Cushman
    Director Global Post Market Surveillance
    Halyard Health

    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:

    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