Joint Action on Reinforced Market Surveillance for Medical Devices and In-vitro Devices - JA from the EU4Health Program
JAMS 2.0 is a Joint Action from the EU4Health Programme. It aims to reinforce the market surveillance of medical devices between Member States and to harmonise approaches across the European Union.
The Joint Action is divided in 8 Work Packages and is comprised of 24 Competent Authorities across Europe.
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Co-funded by the European Union. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or the European Health and Digital Executive Agency (HaDEA). Neither the European Union nor the granting authority can be held responsible for them.
Joint Action on Reinforced Market Surveillance for Medical Devices and In-vitro Devices - JA from the EU4Health Program
JAMS 2.0 is a Joint Action from the EU4Health Program. It aims to reinforce the market surveillance of medical devices between Member States and to harmonise approaches across the European Union.
The Joint Action is divided in 8 Work Packages and is comprised of 24 Competent Authorities across Europe.
--
Co-funded by the European Union. Views and opinions expressed are however those of the author(s) only and do not necessarily reflect those of the European Union or the European Health and Digital Executive Agency (HaDEA). Neither the European Union nor the granting authority can be held responsible for them.
Competent Authorities for Medical Devices