Legalisation Certificate of a Medicinal Product
Since March 29, 2019 the European Medicines Agency (EMA) has relocated to Amsterdam. The documents, including the Certificate of a Medicinal Product (CMP) that is considered to be used abroad shall be legalised in the Netherlands by the Dutch authorities. Certificates that were issued in the United Kingdom before March 29, 2019 can also be legalised in the Netherlands.
JuridConsult can assist you by taking care of the legalisation of a Certificate of a Medicinal Product that is issued by the European Medicines Agency.
What is a Certificate of a Medicinal Product for?
Certificates of a Medicinal Products are issued by the EMA to certify a medicinal product after it has been authorised by the European Commission. The certificate also shows that the manufacturer of the medicinal product complies with the good manufacturing practice.
Why is the legalisation necessary?
The legalisation certificate of a medicinal product is necessary in order to use the document abroad. This document is issued in the Netherlands by the Dutch authorities and can be used abroad only once. We can arrange legalisation of the certificate of a medicinal product by the Ministry of Foreign Affairs and the Court within one working day. Embassy legalisation for the documents that are considered to be used in the countries not parties to the Apostille Convention is also possible (check page Embassy Legalisation).