Press release
Euro Biom Publishes Free Import-Documentation Resources for Overseas Hospital Buyers
London, United Kingdom, 21 June 2026 - Euro Biom Ltd, a UK MHRA-licensed pharmaceutical wholesale exporter, has published a set of free, buyer-facing reference resources to help hospital pharmacies, Ministry of Health procurement teams and licensed distributors across the GCC, Africa, Turkey and Asia navigate the documentation required to import UK-licensed medicines.Procurement teams sourcing UK-licensed medicines routinely face a documentation burden that varies sharply from one destination market to the next. A single shipment may require a Certificate of Pharmaceutical Product (CPP), proof of Good Manufacturing Practice (GMP) status, a free-sale certificate and a destination-country import permit, each issued by a different authority and formatted to a different national standard. Since the UK left the European Union, the paperwork chain for UK-origin medicines has changed, and many overseas buyers report uncertainty over which documents UK suppliers can provide and in what form.
Euro Biom's new resources are designed to remove that friction at the start of the sourcing process rather than at the border. The three resources are free to use, require no registration and are aimed squarely at the people who assemble import dossiers:
A UK Medicine Import Documentation guide explaining CPP, GMP, free-sale and permit requirements for UK-licensed products: https://eurobiom.co.uk/uk-pharmaceutical-import-documentation
A Regulator Comparison tool covering 39 medicines regulators across the markets Euro Biom supplies: https://eurobiom.co.uk/regulator-comparison
A 142-term Pharmaceutical Glossary of import, wholesale and regulatory terminology: https://eurobiom.co.uk/pharmaceutical-glossary
"Buyers tell us the hardest part of sourcing from the UK is not finding the medicine, it is assembling the correct paperwork for their own regulator," a Euro Biom spokesperson said. "We deal with that documentation on every shipment, so publishing it as a free reference was a natural step. The goal is to make UK-licensed supply easier to plan, whether or not a buyer ever works with us."
The resources arrive at a point of structural change in several of Euro Biom's core markets. In Saudi Arabia, the National Unified Procurement Company (NUPCO) has tightened its 2026 tender rules to favour SFDA-approved, locally manufactured products, which raises the documentation bar for imported supply and makes clear, well-evidenced dossiers more important than ever for the categories that still rely on overseas sourcing.
Euro Biom supplies UK-licensed, MHRA-authorised medicines only. Its work covers named-patient import supply, where the buyer's destination-country route is used to bring in a UK-licensed product, drug-shortage supply, GDP-compliant cold-chain logistics, oncology and specialty supply, and tender, NGO and government supply across more than 40 countries.
Euro Biom Ltd
Unit-5 Skyport Drive, Harmondsworth, London UB7 0LJ, United Kingdom
Telephone: +44 7492 670948
Email: work@eurobiom.co.uk
Press contact: Akhlesh Mathur, Director
Euro Biom Ltd is a UK MHRA-licensed pharmaceutical wholesale exporter (Wholesale Dealer Authorisation WDA(H) 59239, Company No. 15380737), founded in 2024 and based near London Heathrow. The company supplies UK-licensed medicines to hospitals, Ministries of Health, NGOs and licensed distributors across the GCC, Africa, Turkey and the CIS/Asia region. Euro Biom specialises in named-patient import supply, drug-shortage sourcing, GDP cold-chain logistics, oncology and specialty supply, and tender and government supply. More at https://eurobiom.co.uk
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