for medical devices

Based in Switzerland consulting team for your medical device company. 

 

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Located outside of Switzerland

and would like to place your CE-marked medical device on the Swiss market?

We offer services as CH-REP (Swiss Authorized representative) with proper documentation review (including supporting with the CE-marking) and subsequent maintaining compliance.

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Located in Switzerland

We offer services in QA&RA, EU-REP, Clinical Studies in EU member state. 

 

 

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START UP? 

We offer various services in QA&RA and accessing EU market. 

 

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