To help smooth the transition to the new medical devices regulations, the European Commission has launched a revamped Medical Devices section on its website.
The updated website explains the main differences between the current directives and the new regulations on Medical Devices (MDR) and In Vitro Diagnostic Medical Devices (IVDR).
The new regulatory requirements are presented in various sections targeted at manufacturers, importers, health institutions, authorities in non-EU countries and others.
Infographic with deadlines for implementation of MDR and IVDR
For more information, please contact:
Brian Svend Nielsen
bsn@dhigroup.com
Tel +45 4516 9140
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