Relocation of the European Commission website on medical devices

In summer 2019, mdi Europa has reported that the European Commission has restructured its website on medical devices. Since then, manufacturers could retrieve valuable information about EU regulatory requirements under the Medical Devices Directive (MDD) and especially under the Medical Devices Regulation (MDR). 

The Commission now published a notice on the website that the medical devices topic will be transferred to another location under Directorate-General for Health and Food Safety. New information will thus be posted on another website section – view here.

Source: European Commission

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