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Swiss AR Services was founded in Switzerland in 2021 and since day one we have been 100% dedicated to the new challenge as CH-REP between Switzerland and the EU.


As of July 31, 2023, Class I MDR products must be labeled with the CH-REP information directly on the label. The indication of the CH-REP on a document attached to the product is no longer permitted.


The EU has extended the transition periods of the In Vitro Diagnostics Regulation (IVDR) 2017/746 from December 2021, according to this press release. The European Council and the European Parliament have approved the proposal...


As a company in the medical device industry, it is of vital importance to ensure the conformity of your products with the applicable European, as well as Swiss directives. 


coming soon

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