Origin Declaration or an Origin Declaration EUR-MED
Article 21 (“Conditions for making out an origin declaration or an origin declaration EUR-MED”) of the rules of origin protocol of the PEM Convention
The origin declaration or an origin declaration EUR-MED is made by the exporter to self-declare the origin of its product.
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Origin declaration or an origin declaration EUR-MED can be made out by:
- an approved exporter or;
- any exporter provided that the total value of the consignment does not exceed EUR 6 000.
- The exporter makes out an origin declaration or an origin declaration EUR-MED based on information demonstrating that the product is originating, including information on the originating status of the materials used in the production of the product (such as supplier’s declaration).
- The exporter is responsible for the origin declaration or an origin declaration EUR-MED and the information provided being correct and should be prepared to submit all appropriate documents proving the originating status of the products at the request of customs authorities.
How to make out an origin declaration
- The exporter should type, stamp or print the following declaration (as mentioned Annex IVa) on the invoice or any other commercial document which describes the products concerned in sufficient detail to enable them to be identified (e.g. delivery note or packing list):
The exporter of the products covered by this document (customs [or competent governmental]
authorisation No … (1)) declares that, except where otherwise clearly indicated, these products are of
… preferential origin (2).
................................................... (3) (Place and date)
....................................................(4) (Name (in clear script) and signature of the exporter)
(1) Put your approved exporter authorization number (for consignments above €6 000).
(2) Put the origin of your product, either EU or the free trade partner country.
(3) Place and date, if not otherwise indicated on the invoice/document.
(4) Name (in clear script) and signature of the exporter. An approved exporter may, within the scope
of his authorisation, be waived from the obligation of signature and in so doing does not need to give the name
of the signatory.
How to make a EUR-MED origin declaration
- In this case, the declaration is the following (Annex IVb)
The exporter of the products covered by this document (customs [or competent
governmental] authorisation No … (1)) declares that, except where otherwise clearly
indicated, these products are of … preferential origin (2)
- cumulation applied with … (name of the country/countries)
- no cumulation applied (3)
...................................................... (4) (Place and date)
.......................................................(5) (Name (in clear script) and signature of the exporter)
(1) Put your approved exporter authorization number (for consignments above €6 000).
(2) Put the origin of your product, either EU or the free trade partner country.
(3) Complete and delete when necessary
(4) Place and date, if not otherwise indicated on the invoice/document.
(5) Name (in clear script) and signature of the exporter. An approved exporter may, within the scope of
his authorisation, be waived from the obligation of signature and in so doing does not need to give the name of
the signatory.
- Further explanations on when to use the origin declaration and EUR-MED origin declaration are provided on page 87 of the handbook
- The declaration can be made in any official language of the EU or official languages of the FTA trade partner according to the language versions in the Annex IVa and IVb
Validity and record keeping.
- Proof of origin is valid for 4 months after the date invoice declaration was made out and needs to be submitted within that period to the customs authorities in the importing party
- A copy of the origin declaration or an origin declaration EUR-MED and other relevant documents need to be kept for at least 3 years by the exporter
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