We provide both external and in-house legalisation support services for your healthcare documents, taking them on securely to the relevant authorities. We also prepare and complete applications for submission to the MHRA, HPRA, EMA, DOH, BIS and DEFRA as well as
Typical documents we process include:
• EMA CPP Certificates
• MHRA CPP Certificates
• GMP Certificates
• Manufacturing Licenses
• Free Sale Certificates
• BIS Certificates
• VMD Certificates
• EMA Commission Reports
• HPRA Certificates
CDN has a dedicated department to assist Pharmaceutical Companies with the application of licence certificate submissions to the MHRA, EMA & HPRA.
We train on your in house procedures and then transfer the systems back to our headquarters. Our fully trained staff understand the sensitivity of the product information and your deadlines.
We process the applications in our secure department and fully check all certificates on their return. This works hand in hand with our legal team here who then proceed to obtain notorisation, apostille and embassy legalisation where required.
A complete in house submission and legalisation process under one roof.
Follow this link for information on
Countries Legalisation Requirements
Follow this link to download our
Healthcare Instruction form