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swissdamed Database Needs A Few More Months With UDI Model Now Underway

Swiss modular database taking shape now using Swissmedic Cloud

 
• By Ashley Yeo

Switzerland has been developing a national medical devices database to mirror Eudamed, the EU version that has excluded participation by Swiss companies since the failure of the federal council and European Commission to update the MRA for devices.

By Maxim Gaigul Royalty-free stock illustration ID: 476308105 Computer keyboard, close-up button of the flag of Switzerland. 3D render of a laptop keyboard

Qualitative improvements have been made to swissdamed, the IT system to support application of the Swiss regulations on medical devices and in vitro diagnostic medical devices, leading to go-live dates being deferred by a few months.

Swissdamed − the Swiss Database on Medical Devices – will enable the regulator, Swissmedic, to directly register economic operators using...

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More from Switzerland

Swiss Medtechs Advised To Work On US Tariff Mitigation Strategies

 
• By Ashley Yeo

The US’ 90-day suspension of higher “reciprocal tariffs” will expire on 9 July, raising fears that the 31% tariff rate on Swiss medtech and other goods exported to the US might make a comeback. While the tariff situation changes on an almost daily basis, medtechs should forearm for any eventually, say local business organizations.

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Swiss Move To Prioritize Ambulatory Care In Healthcare Reform

 
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More from Europe

Time For Medtech To Have Its Say On Critical Changes In EU Framework Legislation

 
• By Amanda Maxwell

In revising the foundations of EU product legislation, the European Commission aims to increase harmonization, cut regulatory burdens and promote digital tools to boost compliance and safety.

Bates To Energize UK Office For Life Sciences

 
• By Ashley Yeo

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International Reliance Gets UK MHRA OK In Drive For Agile Pre-Market Regulation – CE Marking Next

 
• By Ashley Yeo

The UK government’s response to MHRA public consultation on risk proportionate device routes to market and physical UKCA markings adds momentum to drive for modern, agile system. Another consultation in late 2025 will propose indefinite recognition of CE-marked devices in Great Britain.