Swiss-Authorised Representative - Verdict Medical Devices
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Swiss-Authorised Representative

A signed mutual recognition agreement (MRA) between the EU and Switzerland by 26 May 2021 does not seem conceivable anymore. This means Switzerland will become a third-party country where Swiss manufacturers need an EU-authorised representative to export their products into the EU. On the other hand, manufacturers in the EU will need a Swiss-authorised representative to import their products into Switzerland.

This leads to an unsettling situation for many importers, distributors and manufacturers. We at Regulatory Globe and EUmediq are specialised to act as EU and Swiss-authorised representative and we are happy to support you in this matter. Get in contact with Regulatory Globe or EUmediq so we can answer your questions and, if desired, support you as your authorised representative.

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