JuridConsult Takes Care Of Legalisation Of Dutch Documents In Order To Use Them In A Foreign Country.
Switch to our professional help today and experience the benefits yourself! We take care of your documents to make them available for use abroad.
Legalisation Certificate of a Medicinal Product | EMA CMP
Since March 29, 2019 the European Medicines Agency (EMA) has relocated to Amsterdam. The documents, including the Certificate of a Medicinal Product (CMP) and Certificate of a Pharmaceutical Product (CPP) 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 or Certificate of a Pharmaceutical Product that is issued by the European Medicines Agency.
Certificates of a Medicinal Products and Certificate of a Pharmaceutical 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.
The legalisation certificate of a medicinal product or legalisation certificate of a pharmaceutical product is necessary in order to use such 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 Dutch Ministry of Foreign Affairs and the Court by means of an Apostille 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).
Need to legalize a pharmaceutical certificate? Our services ensure a professional and swift legalization process. Whether it’s for export, import, or other international purposes, we offer reliable support to ensure your certificate is legalized correctly. Contact us today for more information and trustworthy legalization of your document.
In order to legalise Certificate of a Medicinal product or to legalise Certificate of Pharmaceutical Product the e-document issued by the EMA is sufficient. However e-document shall bear a digital signature of the official and authorized representative of EMA. You can simply submit the e-document to us by email and we will arrange for a hard copy print which will consequently legalised for the purposes to be used abroad.
Apostille can be placed on e-document which then can be recongnized in around 120 countriees world-wide. Before Apostille can be placed the e-document shall be attested by the Dutch Ministry of Foreign Affairs.
JuridConsult offers to legalise Certificate of Medicinal Product or Certificate of Pharmaceutical Product by means of legalising it at the Dutch Ministry of Foreign Affairs and afterwards by means of an Apostille stamp. Such procedure can be arranged in couple of days. For more information on embassy and consular legalisation you can find in the section Apostille.
JuridConsult offers to legalise Certificate of Medicinal Product or Certificate of Pharmaceutical Product by means of legalising it at the Dutch Ministry of Foreign Affairs and afterwards by required embassy of consular section in the Netherlands. Such legalisation takes between 3-10 working days, depending on the resepctive embassy or consular section’s handling time and workload. For more information on embassy and consular legalisation you can find in the section Embassy legalisation.
Get in touch with us!
© 2024 Chent | All Rights Reserved | Privacy Policy | Terms and Conditions
Would you like to know more about legalisation, certificates, apostille, translations or corporate services?
Then request a free call back! Submit your contact information and we will call you back as soon as possible.
