Appointment of Authorised Representative for EU

30-Jun-2016

In preparation for the registration of their first CE-marked IVD product in the European Union, Sienna has appointed an Authorised Representative for that region.

Bioconnexions Consulting Ltd., an experienced team in the IVD market segment, has been appointed to the role for the next 3 years. A European based authorised representative is required by regulatory authorities for any company intending to sell medical devices, including in-vitro diagnostic products, within the EU.

Sienna is pleased to be working with such a knowledgeable and capable partner to fulfil this key requirement.



 
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