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.
CPP, GMP Certificates & EMA Regulatory Documents
CMP, CPP, GMP Certificates & EMA Regulatory Documents
JuridConsult supports pharmaceutical companies with the legalisation of regulatory documents required for international use.
Many pharmaceutical documents issued within the European regulatory system and the EMA (European Medicines Agency) must be legalised before they can be submitted to authorities outside the EU.
We assist with the legalisation of:
Our goal is simple: ensure your pharmaceutical documents are correctly legalised and accepted abroad.
Pharmaceutical companies often need to submit official regulatory documents when registering medicines in other countries. Many authorities require these documents to be legalised before submission.
JuridConsult assists with the legalisation of:
These documents are commonly required for medicine registration, export, and regulatory verification outside the European Union.
Pharmaceutical companies operating in Europe often work within the regulatory framework of the European Medicines Agency (EMA).
When documents related to EMA-authorised medicines are submitted to authorities outside the EU, those authorities may require legalisation to verify the authenticity of the documents.
JuridConsult has experience supporting companies with the legalisation of pharmaceutical documents connected to the European regulatory system.
The Certificate of Pharmaceutical Product (CPP) is one of the most commonly requested documents for international pharmaceutical registrations.
A CPP confirms that:
Many authorities request a legalised CPP before accepting the document in a regulatory submission.
JuridConsult assists companies in ensuring their CPPs are properly prepared and legalised for international use.
Good Manufacturing Practice (GMP) Certificates confirm that pharmaceutical manufacturing facilities comply with recognised quality and safety standards. These certificates are often issued by national regulatory authorities and demonstrate that medicines are produced in accordance with established pharmaceutical regulations.
When pharmaceutical companies submit regulatory documentation to authorities outside the European Union, a legalised GMP Certificate may be required to verify the authenticity of the issuing authority. JuridConsult assists companies with the legalisation of GMP Certificates, ensuring that these documents are properly prepared for international regulatory submissions.
A Free Sale Certificate confirms that a pharmaceutical or healthcare product is legally marketed and sold in its country of origin. Many regulatory authorities request a legalised Free Sale Certificate when products are registered, exported or submitted for approval abroad.
JuridConsult supports pharmaceutical companies with the legalisation of Free Sale Certificates, helping ensure that these documents are properly authenticated and accepted by foreign regulatory authorities.
JuridConsult specialises in the legalisation of pharmaceutical documents for international regulatory use.
Clients choose JuridConsult because we offer:
We help ensure that pharmaceutical documents are prepared correctly and accepted by foreign authorities.
Switch to our professional help today and experience the benefits yourself! We take care of your documents to make them available for use abroad. Thank to our legalisation support, it will be confirmed that the documents were issued by the competent authorities and they will be ready for use abroad.
Do you require more information about legalisation of documents? Do you have any questions about services we offer and our rates? You can get in touch with us here for more information. Fill out contact form or call +31 626 52 3008.
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