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- MedTech
Placing Medical Devices on the Swiss Market After the EU MDR Date of Application
Under the European Union's Medical Devices Regulation (MDR), Switzerland is currently considered a third country for medical devices. Find out what that means for manufacturers and importers, and how to safeguard obtain the proper clearance to place Europe
- EMEA
- MedTechPharmaceuticals / BioTech
European IVDR Application Partially Postponed
European Commission proposes staggered IVDR compliance timelines to address various implementation challenges.