About the Joint Action on Market Surveillance of Medical Devices

The Joint Action on Market Surveillance of Medical Devices (JAMS) aims to reinforce the market surveillance system for medical devices by improving the coordination of activities by all Member States of the European Union, and ensuring adequate communications and cooperation. These are crucial for success and effectiveness of the market surveillance in the field of medical devices.

Find out more about this Joint Action:

  • Overview of Work Packages – Read more about the Work Packages and see what the Joint Action has delivered.
  • Participants – See who has been involved in developing and delivering this Joint Action.

You can also download the “Market Surveillance for Medical Devices” leaflet to find out more about the Joint Action.

The content of this website represents the views of the author only and is his/her sole responsibility; it cannot be considered to reflect the views of the European Commission and/or the Consumers, Health, Agriculture and Food Executive Agency or any other body of the European Union. The European Commission and the Agency do not accept any responsibility for use that may be made of the information it contains.

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