EC New portal will ease transition to medical devices Regulations

8 février 2019

BlueRegWatch

The recently launched Medical Devices section on the European Commission's website was revamped to help smooth the transition to 2 new Regulations on medical devices and in vitro diagnostic medical devices. The portal presents the new regulatory requirements in various sections targeted at impacted actors (manufacturers, importers, health institutions, authorities in non-EU countries and others)…

BlueRegWatch

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