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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

25-26 Jan 2017
Bally's Las Vegas | Las Vegas, NV, United States of America

Conference Workshop

Pre-Conference Workshop on January 24: Implementing a Comprehensive Risk Management Strategy to Achieve and Preserve Regulatory Compliance with Medtronic

Conference Workshop

Pre-Conference Workshop on January 24: Assessing the Post-Market Surveillance Sequence to Underline Opportunities for Improvement with Hill-Rom


Why You Should Attend

5th Annual Medical Device Safety Monitoring and Reporting

The 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 EU regulatory updates to fortify compliance initiatives
  • Analyze proposed FDA metrics requirements to pinpoint regulatory changes
  • Categorize emerging global regulations to achieve regulatory adherence
  • Emphasize the role of Corrective and Preventative Actions (CAPA) for the overall health of quality management systems
  • Consolidate complaint handling systems to reduce response times

  • 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
    Amgen

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

    Roee Lazebnik, MD, Ph.D.
    Vice President, Global Device Medical Organization
    Pfizer

    Tauqeer Karim, MD, MS, MACP, FASN
    Vice President, Drug & Device Safety Officer
    Fresenius Medical Care NA

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

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

    Julie Finke
    Vice President, Quality Systems & Processes
    Roche Diagnostics

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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