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Achieve Success with European Medical Device Commercialization

Whether you are a US company bringing your medical device to market in the European Union, or an EU company commercializing a new product, the regulatory route for medical device approval in the European Union is very manageable – given the right knowledge and tools.

In this paper you will learn about:

  • EU Medical Device Classification
  • Required documentation for commercialization
  • Tips on choosing a Notified Body
  • The importance of Risk Management and Safety Testing

Take a smoother path to commercialization in the European Union…

Contact MethodSense today to get started.

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EU Medical Device White Paper