Named Patient Supply

UK-Based Named Patient
Medicine Supply
for Hospitals & Institutions

Euro Biom is an MHRA WDA-licensed pharmaceutical wholesaler specialising in the sourcing and supply of unlicensed and named patient medicines to hospitals, procurement teams and NGOs in the UK and internationally.

MHRA WDA Licence No. WDA(H) 59239Granted 17 March 2026
Submit a Named Patient Enquiry Read Our Full Guide

⚡ Same-day response to every enquiry  ·  Mon-Fri 09:00-18:00  ·  WhatsApp us

What is Named Patient Supply
When no licensed
alternative exists.

A named patient medicine is an unlicensed medicine supplied for an identified patient when no licensed product is available or clinically appropriate. In the UK, this is permitted under Regulation 167 of the Human Medicines Regulations 2012.

The prescribing doctor takes clinical responsibility for the decision to use the unlicensed product. The supplier, Euro Biom, takes responsibility for sourcing from authorised manufacturers, maintaining the cold chain, and providing complete GDP-compliant documentation.

This service is also used internationally, where a medicine is registered in the UK but not in the destination country, or where the patient requires a specific formulation, strength or presentation unavailable locally.

Regulation 167 HMR 2012 MHRA WDA Licensed GDP Compliant Full Documentation
"When a medicine is unavailable through licensed channels, named patient supply is the legal and regulated pathway. Euro Biom holds the authorisations to execute it correctly."
Who This Service Is For
Built for Institutional
and Clinical Procurement

Named patient supply is used by a wide range of healthcare buyers. If your conventional supplier cannot source what you need, we can.

🏥
NHS Trusts & UK Hospitals
Hospital pharmacists and procurement managers requiring unlicensed medicines for specific patients when the licensed equivalent is unavailable, unsuitable or not registered in the UK. We are an MHRA-authorised supplier for these cases.
🌍
International Hospitals & Clinics
Healthcare institutions in GCC, Africa and beyond requiring medicines registered in the UK but not in their country, or specific branded products unavailable through local distributor channels. We manage UK export documentation throughout.
🏛️
NGOs, Governments & Health Ministries
Procurement teams managing patient programmes or institutional supply that includes medicines outside standard licensed catalogues. We support tender responses, programme-level sourcing and long-term supply arrangements.
Our Authorisations

The licences that make
this supply legal and traceable.

Named patient supply must be handled by an MHRA-licensed Wholesale Dealer. Euro Biom holds the correct authorisations to source, handle and export unlicensed medicines compliantly.

MHRA Wholesale Dealer Authorisation

Euro Biom holds WDA(H) 59239, granted by the Medicines and Healthcare products Regulatory Agency on 17 March 2026. This authorisation is publicly verifiable on the MHRA register.

WDA(H) 59239  |  MHRA Site 37434242

GDP Good Distribution Practice

All products are handled in accordance with UK Good Distribution Practice guidelines. Every shipment includes a complete chain-of-custody record, temperature monitoring where required, and batch-level documentation from manufacturer to recipient.

Full documentation with every supply

Regulation 167, Human Medicines Regulations 2012

UK legislation permits the supply of unlicensed medicines to meet individual patient needs where no licensed alternative is suitable. Euro Biom operates within this framework, supplying only on the basis of a prescriber's clinical decision and documented patient need.

Prescriber responsibility  |  Supplier compliance

International Export

Our WDA authorises export of named patient medicines to countries worldwide. We prepare all UK export documentation including Certificates of Free Sale, and can advise on import requirements for GCC, African and Asian markets based on our operational experience.

40+ countries  |  Export documentation included
How It Works
From Enquiry to Delivery,
Step by Step

Our process is designed to be fast, clear and fully compliant at every stage.

Step 01
01
Submit Your Requirement
Send us the medicine name, strength, formulation, quantity, destination country and any urgency or clinical context. We respond the same working day.
Step 02
02
Sourcing Assessment
We identify authorised manufacturers or distributors, confirm availability and present sourcing options with indicative lead times. No obligation at this stage.
Step 03
03
Documentation and Compliance
Once confirmed, we prepare all required GDP documentation, export licences, Certificates of Analysis, and any country-specific import paperwork.
Step 04
04
Shipment and Delivery
Product is dispatched via specialist pharmaceutical logistics with full tracking, temperature monitoring where required, and customs clearance support for international orders.
Where Named Patient Supply Is Most Used
Therapeutic Areas We Supply

Named patient requirements arise most frequently in specialty and rare disease medicine. Euro Biom has experience across all of the following therapeutic categories.

🔬
Oncology
Unlicensed chemotherapy, targeted therapies and supportive care for cancer patients where licensed supply has failed or is unavailable locally.
🧬
Immunology and Transplant
Immunosuppressants and biologic therapies for transplant patients or rare autoimmune conditions, often unavailable through conventional UK distribution.
🧠
Neurology
Specialist anticonvulsants, Parkinson's therapies, MS disease-modifying treatments and neuropathic pain agents not commercially available in the UK.
🫀
Rare and Orphan Diseases
Medicines for rare diseases where commercial manufacturing is limited, global supply is restricted, or the product has not been registered in the destination market.
🩸
Haematology
Clotting factors, EPO, iron infusions and specialist haematology medicines for patients with complex requirements beyond standard licensed supply.
💊
Any Other Therapeutic Area
Named patient supply applies across all medicine categories. If your required product is not listed here, submit an enquiry and we will assess the sourcing pathway.
Submit an Enquiry
What to include
for the fastest response.

The more detail you provide upfront, the faster we can assess sourcing options and respond with availability and lead times. None of these fields are mandatory to start, but each one speeds up the process.

Submit a Named Patient Enquiry →

⚡ Same-day response  ·  WhatsApp us directly

1
Medicine name (INN or brand)
International Non-proprietary Name preferred. If brand, include country of origin if known.
2
Strength and formulation
e.g. 10mg tablets, 100mg/5ml oral solution, 50mg/ml injection.
3
Quantity required
Pack size and number of packs, or total units. Indicate if this is a recurring requirement.
4
Destination country
Required for export documentation and to assess any import restrictions at the destination.
5
Urgency and required date
Emergency, urgent or routine. Any firm deadline drives our sourcing prioritisation.
6
Clinical or procurement context
Optional but helpful. Reason for named patient supply, prescriber details or programme context.

Ready to Submit a Named Patient Enquiry?

Tell us what you need. We respond the same working day with sourcing options, availability and lead times. No commitment required at enquiry stage.

Frequently Asked Questions
Named Patient Supply, Explained

Common questions from hospital pharmacists, procurement managers and international buyers.

What is a named patient medicine?
A named patient medicine is an unlicensed medicine supplied for a specific, identified patient when no licensed alternative is available or suitable. In the UK, this is permitted under Regulation 167 of the Human Medicines Regulations 2012.
Who can supply named patient medicines in the UK?
Named patient medicines must be supplied by an MHRA-licensed Wholesale Dealer. Euro Biom holds WDA(H) 59239, authorising us to procure, supply and export unlicensed medicines through legally compliant regulatory pathways.
How quickly can you source a named patient medicine?
Timelines depend on the medicine, its origin and your location. For stocked or readily available products, supply can be arranged within days. For more complex sourcing, we give an honest timeline at the point of enquiry. We respond to all enquiries the same working day.
What documentation comes with named patient supply?
Every supply includes a Certificate of Analysis, batch records, transport and temperature records where applicable, and all export or import documentation required for your destination country. Full GDP-compliant paperwork as standard.
Can you supply named patient medicines internationally?
Yes. We export named patient and unlicensed medicines to hospitals, governments and NGOs across 40+ countries, including GCC states, Africa and Asia. Our MHRA WDA covers export, and we manage all UK export documentation as part of the service.
Are there medicines you cannot supply?
Our scope is broad, but some medicines are subject to additional restrictions such as controlled drug legislation or manufacturer allocation controls. If we cannot supply a product, we will tell you at the enquiry stage and suggest alternatives where possible.