The European Commission It issued a document concerning the consequences of Brexit over Europe trade of products from the United Kingdom.
The document covers all the products introduced in the European Community, excluding food and agricultural, from the date of 30 March 2019, date that will be the release of the UK from the European Community (unless extended).
The committee emphasized that, starting from the release date, manufacturers and importers established in the UK will no longer be considered operators established in the European Community.
The result is that a business established in any other member country, that before the Brexit was considered a distributor, It will automatically become an importer and will be subject to the Law on products from third countries.
In practical terms, he will have to fulfill the obligations of importers which are different from those distributors.
There is more. European regulations concerning products will no longer recognize authorized representatives established in the United Kingdom. So the non-EU companies that today employ an authorized representative (or agent) for placing their products in the European market, will relocate this function to another of EU countries.
Also according to the document, Notified Bodies UK will not be so for the European law and will not be allowed to comment on the CE certification of products the conditions laid down in Union harmonization legislation.
What will make people working in the field?
They must be assured that any appraisal certificate (EU type examination) comes from a notified entity one of the Community's member countries.
The manufacturer will still have to keep updated EC declaration of conformity of its products and ensure that the responsible for placing on the market lies in the European Community.
Sempre nell’ambito dei cambiamenti post Brexit anche l’Agenzia Europea per i Medicinali e l’Autorità Bancaria Europea dovranno lasciare le proprie sedi nel Regno Unito e trasferirsi in uno dei paesi della commissione entro il 30 March 2019.
Per quanto riguarda l’Agenzia Europea per i Medicinali (EMA), in data 20 November 2017, il Consiglio europeo ha scelto Amsterdam come nuova collocazione.
However, the Italian Government has asked to cancel this decision, stressing that there would be “ensuring that the Agency can be operational and fully functional from the release date of the United Kingdom European Union (30 March 2019), taking into account the need for space and adequate logistical solutions for offices, the meeting rooms, archives and the appropriate safety standards of infrastructure”.
The European Banking Authority (EBA) It will be transferred to Paris.
The decision was determined by the draw after the third round of voting. In the third round had come Paris and Dublin.
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