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Challenges with Global Labeling Compliance in the Medical Device Industry

Increase Labeling Process Efficiency through Content Management Systems, Closer Following of International Guidelines, and Improved Translation

24-25 Jan 2017
NBC TOWER | Chicago, IL, United States of America


Why You Should Attend

Challenges with Global Labeling Compliance in the Medical Device Industry

Medical Device manufacturers are facing growing challenges from regulatory bodies around the globe for better translation, country by country reporting and rapidly updated labels. Content management systems and other increased technology can assist in overcoming day to day challenges that labeling teams will face.

 

Key Topics

  • Enhance Labeling Processes to Increase Competitive Edge
  • Combat Label Translation Issues
  • Implementing a Content Management System
  • Country of Origin and Trade Compliance in Labeling
  • Symbols, Markings, and Content


    • 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

    Lena Cordie
    Consultant | Qualitas Professional Services, LLC
    She has over 20 years of quality and project management experience including 10 years in project management at Target Financial Services and 11 years as Director of Operations at Key Surgical. As a consultant at Qualitas Professional Services, LLC, Ms. Cordie now focuses on helping companies implement quality management systems, UDI solutions for labelling and FDA GUDID submissions, and providing validation, documentation and project management resources to global medical device companies. She is an active member of AAMI, ISO - ISO/TC 198 (ISO 17664 & ISO 11139) and ISO/TC 210 (ISO 13485 & ISO 15223) working groups as well as RAPS.

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    Event Contact

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

    Emily Jones

    marcusevans, The NBC Tower
    455 N. Cityfront Plaza Dr.
    Chicago, IL 60611

    Telephone:     312.540.3000 x6714
    Fax: 312.894.6304
    Email: emilyj@marcusevansch.com