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The Latest Developments in Europe’s Regulation of Medical Devices and Projections for 2014
The Latest Developments in Europe’s Regulation of Medical Devices and Projections for 2014


 
Our Price: $395.00

Product Code: WB-7065
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About the Product
Includes 1 hour and 25 minute Windows Media Video File and PowerPoint presentations for immediate download.


In order to best protect patients and healthcare providers within the European Union, and with a focus on creating a unified system for regulatory oversight of medical devices, EU policy makers have proposed and enacted a variety of new regulatory oversights of these innovative and important products. Understanding the methods by which decisions are made and new regulations are enacted is critical as medical device manufacturers look for a compliant and clear path for moving forward. Through an in-depth analysis of the European regulation of medical devices, and recent cases impacting the regulatory environment, participants will have a clearer understanding of the current regulations as well as projections into the new year.
  • Key players and responsibilities: Council, ENVI committee, notified bodies, competent authorities
  • Timescales and impacts on innovation: Upcoming proposals, debates, votes and implementation
  • Analysis of Lycocentre case and effects on harmonization

Speaker:
Erik Vollebregt
Lawyer and Founding Partner
Axon Lawyers


Participants that will find this webinar most beneficial will be those involved in medical device companies. Job titles of attendees that will be most applicable for this session will be:

  • Regulatory Affairs
  • Legal Counsel
  • Quality Assurance


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