For Pharmaceutical Manufacturers

Pharmaceutical Manufacturer
Distribution Arrangements

Euro Biom is an MHRA WDA-licensed UK distribution partner for pharmaceutical manufacturers. Exclusive territory deals, hospital channel access, regulatory liaison and international export to over 40 markets, run from a Heathrow-adjacent operation.

MHRA WDA Licence No. WDA(H) 59239Granted 17 March 2026
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What Is a Distribution Arrangement
A regulated route
to UK and 40+ markets.

A manufacturer distribution arrangement is a contractual agreement under which an authorised wholesaler holds, distributes and supplies the manufacturer's products into specified markets. The arrangement may be exclusive, granting one distributor sole rights to a territory or customer segment, or non-exclusive, where multiple wholesalers operate alongside one another.

For manufacturers entering the UK or expanding into the GCC, Africa or CIS markets, the right distribution partner shortens time-to-revenue, isolates the manufacturer from in-country regulatory complexity, and provides direct access to hospital procurement teams, tender frameworks and named patient demand.

Euro Biom partners with manufacturers whose products serve hospital pharmacy, named patient supply, Specials, oncology, transplant immunology and rare disease segments. Our value is the combination of MHRA licensing, Heathrow logistics, an active customer base in 40+ countries, and a regulatory team that has executed UK and international supply for clinically demanding product categories.

MHRA WDA(H) 59239 GDP Compliant Heathrow-Based 40+ Markets Active
"A manufacturer's UK distributor is a regulatory partner first and a commercial partner second. Euro Biom holds the licences, the documentation discipline and the customer relationships to be both."
Why Manufacturers Choose Euro Biom
Built for Regulated
Pharmaceutical Distribution

Three structural advantages drive most of our manufacturer partnerships. Each is a direct consequence of how Euro Biom is set up.

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MHRA WDA Credentials
WDA(H) 59239 covers procurement, supply and export. MHRA Site 37434242. Granted 17 March 2026 with a Responsible Person on the licence and contract warehousing through an audited GDP partner. Publicly verifiable on the MHRA register, ready for manufacturer due diligence.
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Heathrow Logistics Advantage
Our operation sits two miles from London Heathrow. International export shipments transition from warehouse to airline cargo in hours, not days. Cold chain integrity is preserved across short ground legs, and customs clearance partnerships are already in place for our most active export corridors.
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40+ Active Market Access
Live customer relationships across GCC (Saudi Arabia, UAE, Qatar, Kuwait, Bahrain, Oman), Africa (Nigeria, Kenya, Ghana, South Africa, Egypt, North and West Africa), CIS, Asia and Europe. A manufacturer's product reaches multiple territories through one regulatory and commercial relationship.
What We Provide Manufacturers

Service offerings that
extend beyond logistics.

A distribution partner is more than a warehouse. We provide the full operational, regulatory and commercial wrapper that lets a manufacturer focus on production while we handle UK and international market access.

Exclusive Territory Distribution

Country, regional or customer-segment exclusivity for products where a single trusted distributor adds more commercial value than open-market wholesale. Exclusivity windows are aligned with manufacturer launch plans and supported by reasonable minimum-volume commitments where appropriate.

UK, GCC, Africa  |  Bespoke commercial terms

Hospital and Tender Channel Access

Direct relationships with NHS trust pharmacies, private hospital groups, ministry of health procurement teams across the GCC, and major NGO and tender platforms in Africa. Your product is presented through the channel each market trusts, with quotation and tender response handled by our team.

NHS  |  MOH tenders  |  NGO frameworks

Regulatory Liaison and Dossier Support

Where required, we coordinate with destination-country regulatory authorities, support import licence applications, prepare Certificates of Free Sale, and act as the documented importer of record. We do not act as Marketing Authorisation Holder, but we hold the operational licences that make the distribution leg of the regulatory chain compliant.

Import licences  |  CFS  |  Importer of record

GDP Storage, Distribution and Cold Chain

UK Good Distribution Practice from receipt to dispatch. Temperature-controlled storage including 2 to 8 degree cold chain, validated transport solutions for cross-continent shipping, batch traceability, recall capability tested annually, and complete audit-ready documentation for every transaction.

GDP  |  Cold chain validated  |  Audit-ready
How Onboarding Works
From Discovery to Activation,
in Four Stages

Standard onboarding runs 6 to 10 weeks. The stages are predictable, and the manufacturer's regulatory team has visibility into every checkpoint.

Stage 01
01
Discovery
Initial commercial discussion. Product portfolio, target markets, exclusivity scope, expected volumes, and timeline. Mutual NDA in place within 48 hours. Indicative commercial terms within 10 working days of the introductory call.
Stage 02
02
Due Diligence
Two-way regulatory due diligence. We share our WDA, MHRA inspection history and Quality Manual. Manufacturer shares GMP certificate, Site Master File and Quality Technical Agreement template. Site visit or virtual GDP audit where required.
Stage 03
03
Agreement
Distribution agreement and Quality Technical Agreement signed. Pricing, exclusivity scope, minimum commitments, intellectual property, recall responsibility and termination provisions documented. Reviewed by both legal teams.
Stage 04
04
Activation
First inbound shipment. Warehouse receiving and quality release. Customer announcement to active accounts in scope markets. First commercial supply executed under the agreement. Quarterly governance review schedule established.
Manufacturer Types We Work With
Where Our Distribution
Adds the Most Value

Our partnership profile is concentrated where regulatory complexity, hospital sales motion and international supply combine. The following manufacturer types most often benefit from a partnership with Euro Biom.

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Specials Manufacturers
UK MS-licensed Specials manufacturers seeking distribution into hospital pharmacy and community pharmacy channels. We extend your reach without you needing to maintain a UK-wide commercial team.
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Generic Manufacturers
UK and international generic manufacturers entering the UK or expanding into the GCC and Africa. Strong fit where the product addresses a known shortage or named patient demand pocket.
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Branded Specialty
Branded specialty manufacturers in oncology, transplant immunology, rare disease and high-cost specialty therapy. Hospital channel sales execution combined with international tender access.
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Biotech and Biologics
Biotech and biologics companies with cold-chain-sensitive products requiring validated 2 to 8 degree handling, extended supply chain custody and competent regulatory liaison in destination markets.
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Overseas Manufacturers
EU, US, Indian and Middle East manufacturers seeking UK or onward GCC and African market entry without setting up an in-country subsidiary. Our WDA acts as the regulatory bridge.
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Contract Manufacturers
CMOs and CDMOs holding finished product on behalf of brand owners, where the brand owner is seeking a separate downstream UK or international distribution partner under a tripartite arrangement.
Documentation We Handle
Compliance paperwork,
handled end-to-end.

Manufacturer distribution arrangements live or die on documentation discipline. Euro Biom prepares, holds and exchanges the regulatory and commercial paperwork that keeps the relationship audit-ready and the supply chain compliant. Below is what we manage on every active partnership.

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1
WDA documentation pack
Our MHRA Wholesale Dealer Authorisation, Site licence reference, Responsible Person details and inspection history made available for your due diligence.
2
GDP audit and Quality Manual
Quality Manual, SOPs covering goods-in, storage, picking, dispatch, recall and deviation. Available for review or virtual audit prior to signing.
3
Quality Technical Agreement
Quality Technical Agreement covering responsibilities for batch release, complaints, recall, change control and audit rights, signed alongside the commercial agreement.
4
Distribution agreement
Commercial distribution agreement with pricing, exclusivity scope, minimum commitments, intellectual property treatment and termination provisions.
5
Import and export licences
UK import documentation for inbound product, export licences and Certificates of Free Sale for outbound shipments to GCC, African and CIS destinations.
6
Batch records and CoCs
Per-batch traceability documentation, manufacturer Certificate of Conformity, transport temperature records, and customer-side proof of delivery on every transaction.

Ready to Discuss a Distribution Partnership?

Send us your product portfolio outline, target markets and timeline. We respond the same working day with an initial commercial view, indicative terms and the next-step path. Mutual NDA available within 48 hours.

Frequently Asked Questions
Manufacturer Distribution, Explained

Common questions from pharmaceutical manufacturers, business development teams and external regulatory advisors.

What is a manufacturer distribution arrangement?
A contractual agreement under which an authorised wholesaler holds, distributes and supplies the manufacturer's products into specified markets. Arrangements may be exclusive or non-exclusive and are governed by GDP, GMP and the regulatory law of each market served.
Do I need a UK distributor for the UK market?
Most manufacturers entering the UK work through an MHRA-licensed UK distributor for at least the launch phase. The distributor handles WDA-compliant storage, hospital procurement engagement and operational logistics. Whether the arrangement is exclusive or non-exclusive depends on commercial strategy.
What credentials does Euro Biom hold?
MHRA WDA(H) 59239 granted 17 March 2026. MHRA Site 37434242. Operating from Unit 5 Skyport Drive, Harmondsworth, two miles from Heathrow. Procurement, supply and export scope, full GDP compliance, and contract warehousing through Clarity Pharma Ltd.
Can you export to international markets?
Yes. Our WDA covers export, with active distribution to over 40 countries across the GCC, Africa, CIS and Europe. Manufacturers can reach multiple territories through one regulatory and commercial relationship rather than appointing a distributor in each country.
How long does manufacturer onboarding take?
Standard onboarding runs 6 to 10 weeks from initial discussion to first commercial supply. Faster onboarding is possible for manufacturers already supplying into the EU under audited GMP. The timeline covers due diligence, GDP audit, agreement drafting and warehouse activation.
What documentation do you require from the manufacturer?
GMP certificate, current Site Master File or equivalent, product specification sheets including SmPC and PIL where licensed, batch release procedure, recall procedure, and a Quality Technical Agreement covering the distribution scope.
Are exclusivity arrangements available?
Yes. We offer country, regional or customer-segment exclusivity where this serves the manufacturer's commercial strategy. Exclusivity is supported by reasonable minimum-volume commitments and termination provisions to protect both sides.