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5th Annual Medical Device Safety Monitoring and Reporting

Fortifying Post-Market Surveillance to Expedite Compliant Handling and Reinforce Patient and Product Safety

24-26 Jan 2017
Las Vegas, NV, United States of America

Why You Should Attend

5th Annual Medical Device Safety Monitoring and Reporting

Product safety is the number one priority of medical device manufacturers. At a time when methods of communication are constantly evolving and expanding and information is ubiquitous, it is challenging, yet necessary, for medical device companies to manage large data streams, be alerted of product malfunctions, and respond efficiently to customer complaints. Coupled with continually changing and ever more stringent regulatory requirements, it is an uphill battle for many medical device manufacturers to manage a harmonized and integrated safety, surveillance, and reporting strategy.

This marcus evans 5th Annual Medical Device Safety Monitoring and Reporting conference aims to shed light on FDA and international guidelines on medical device monitoring and reporting, as well as benchmark best practices from peers across the industry. Delegates will receive practical knowledge and tangible tactics from leading regulatory affairs, compliance, quality assurance, and post-market surveillance professionals on how to efficiently collect and effectively house post-market data, streamline the reporting process to ensure deadlines, and maximize existing tools and technologies to gather all necessary product information.

Key Topics

  • Forecast impacts from FDA regulatory updates to fortify compliance
  • Analyze proposed FDA metrics requirements to pinpoint regulatory
  • Categorize emerging global regulations to achieve regulatory
  • Promote increased risk management to ensure audit-preparedness
  • Emphasize role of CAPA for the overall health of quality

  • 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 Sponsors
    Silver Sponsor
    Pilgrim Quality Solutions
    Visit website >>

    Event Partners

    Practical Insights From

    Thomas Bento
    Sr. Vice President of Quality & Regulatory Assurance
    Nihon Kohden America

    Maureen Ellis
    Director, Chemistry Manufacturing Controls / Device Safety

    Joseph M. Purpura, MD, MS
    Senior Medical Director, Head of Device Safety, Global Patient Safety & Epidemiology

    Dick Roy
    Product Surveillance Director
    GE Healthcare

    Patrick Caines, Ph.D.
    Senior. Director, Quality & Compliance
    Baxter Healthcare Corporation

    Dennett F. Kouri, Jr., JD
    Sr. Director, Quality, Regulatory, Clinical
    Edwards Lifesciences, LLC

    Michele Donatich R.N.
    Director Product Quality & Regulatory Compliance
    Cardinal Health

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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

    312-540-3000 Ext: 6310
    Fax: 312-540-3000 Ext: 6327