Supplier Qualification
Pack
Everything a procurement team needs to qualify Euro Biom as a supplier, in one place.
Before a first order, hospital, Ministry of Health, NGO and distributor buyers must vet a supplier on three points: a valid MHRA Wholesale Dealer Authorisation, Good Distribution Practice compliance, and a verifiable registered company. This page consolidates Euro Biom's real, independently checkable trust artifacts so that qualification is frictionless. Euro Biom is a UK MHRA WDA-licensed wholesale exporter and supplies UK-licensed, MHRA-authorised finished medicines only.
Independently.
Each credential below can be confirmed directly with the regulator or registry. You are not relying on our word. These are the first checks any procurement or compliance team should run before onboarding a pharmaceutical supplier.
Wholesale Dealer Authorisation
The Medicines and Healthcare products Regulatory Agency licence that permits a UK company to wholesale and export medicines. Holding a valid WDA(H) means the company is inspected by the MHRA and operates to Good Distribution Practice. The MHRA register is a public search tool, so you can confirm the authorisation directly with the regulator.
Search the MHRA register for WDA(H) 59239Registered Company Status
Euro Biom Ltd is registered in England and Wales under company number 15380737 and was founded in 2024. The Companies House public register shows the registered office, officers and filing history. Confirming corporate registration alongside the MHRA licence lets a buyer verify both legal status and regulatory authorisation.
View on the Companies House registerGood Distribution Practice
Good Distribution Practice is the UK and EU standard for the storage, handling and transport of medicines, including cold-chain products held within 2 to 8 degrees Celsius. GDP compliance is a condition of holding the WDA(H) and underpins every shipment. Our compliance page sets out the standards we work to across procurement, storage and export.
Read our compliance standardsNamed GDP Oversight
Every WDA(H) holder must appoint a named Responsible Person who oversees Good Distribution Practice and is accountable to the MHRA. For Euro Biom, a named Responsible Person carries that role. To protect against impersonation, the individual's name is not printed here; it is disclosed in the full qualification pack and on request to a verified buyer.
Request the named Responsible PersonTake Away Today.
These documents are public and ready to download for your vendor file, tender bid or onboarding pack. No sign-up required.
Company Profile
An overview of Euro Biom, our WDA scope, markets served and supply capabilities, suitable for a vendor file or first introduction to a procurement team.
Signed Quality Policy
Our signed quality policy setting out the commitment to Good Distribution Practice and quality management that governs how we procure, store and export medicines.
UK Medicine Import Guide
A practical guide to importing UK-licensed medicines, covering the documentation set, regulatory routes and the steps buyers in the GCC and Africa most often ask about.
Quality Policy
Read our quality policy and quality management commitments online, summarising the standards behind every order Euro Biom fulfils.
Modern Slavery Statement
Our modern slavery and ethical supply statement, increasingly required in vendor onboarding and tender compliance documentation.
Need Something Else?
If your tender or onboarding requires a document not listed here, send us the checklist and we assemble the matching pack for your bid.
Never Publish.
Some qualification items are sensitive and are shared securely only after a verified enquiry, never posted on a public web page. This protects both you and Euro Biom from payment fraud and supplier impersonation.
- Bank and payment detailsShared securely and confirmed directly, never published or sent by unsolicited message.
- Full KYC and due-diligence packKnow-your-customer documentation provided directly to a verified buyer or procurement team.
- Signed WDA certificate copyA copy of the signed authorisation, supplied on request to support your vendor file.
- Batch-specific certificatesCertificate of Analysis and batch release tied to the exact stock on your order.
Answered.
The questions procurement, compliance and registration teams most often ask when qualifying a UK pharmaceutical supplier.
Request our full qualification pack.
Send us your vendor onboarding checklist or tender document list and we return the matching pack, including the confidential items shared securely after a verified enquiry. Same-day response to every enquiry.
Further tools and references for procurement teams, registration leads and hospital pharmacists vetting and ordering from a UK pharmaceutical supplier.