Danish regulator issues guidelines on new Eudamed registration requirements
This article was originally published in RAJ Devices
Executive Summary
The Danish Medicines Agency has released information regarding the more stringent registration requirements for medical devices that came into force on 1 May 2011, when Eudamed, the European databank for medical devices, became mandatory throughout the EU1,2.
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Danish regulator issues guidelines on new Eudamed registration requirements
The Danish Medicines Agency has released information regarding the more stringent registration requirements for medical devices that came into force on 1 May 2011, when Eudamed, the European databank for medical devices, became mandatory throughout the EU.
Denmark raises fees for device manufacturers
The Danish Medicines Agency (DMA) has raised its medical device registration fees, three years after the last fee increase. The new fees, which have gone up by about 1.5%, came into effect on January 4.
Denmark raises fees for device manufacturers
The Danish Medicines Agency has raised its medical device registration fees1. The new fees, which have increased by about 1.5%, came into effect on 4 January.