Global pharmaceutical distributor for authorised importers worldwide

GPD operates as an MHRA-licensed pharmaceutical wholesaler and exporter, coordinating international pharmaceutical distribution from the UK for authorised importers, NGO procurement teams and health ministry buyers.

In short: GPD prepares export-ready consignments in the UK and hands them over to the buyer’s authorised importer. The importer manages regulatory clearance and national distribution with its own regulator. GPD does not hold local representation in destination countries.

Discuss an export order

See who does what

International pharmaceutical distribution from the UK

GPD coordinates international pharmaceutical distribution from the UK for authorised importers and institutional buyers. Each consignment is prepared with export documentation, certificates of analysis and batch traceability records, with temperature-controlled storage and validated packaging supporting cold chain integrity in transit.

The export operation runs under the same MHRA licence as GPD’s work as a UK pharmaceutical wholesaler.

Who does what in an international order

Clear roles keep export orders compliant. This is how responsibility is split between GPD, the logistics partner and the authorised importer.

Stage	Handled by	GPD's part
Product sourcing and verification	GPD	Buys only from approved suppliers and checks authenticity before accepting stock.
GDP storage in the UK	GPD	Holds stock in monitored, temperature-controlled storage.
Export documentation	GPD	Prepares certificates of analysis, batch traceability records, temperature logs and export documentation.
International transit	Validated logistics partner	Coordinates temperature-controlled handling and passes monitoring data to the importer.
Regulatory clearance in the destination country	Authorised importer	Provides the records the importer needs for its submission.
National distribution	Authorised importer	No role. GPD does not distribute within destination countries.

How an export order moves from the UK

Share the destination brief

The buyer or importer shares the products, quantities, destination and any temperature requirements.

Confirm the authorised importer

GPD confirms which authorised importer will receive the consignment and what documentation its regulator expects.

Align the documentation

GPD prepares the documentation set to match the requirements the importer works to.

Prepare and pack

Stock leaves GDP storage in validated packaging, with temperature monitoring devices fitted where required.

Hand over the records

The consignment travels with its batch records and temperature data, so the importer can verify it on arrival.

Documentation aligned with destination regulators

Each authorised importer works to its own national regulator. GPD aligns export documentation with the requirements the importer sets. Regulatory approval stays with the importer in every case.

Market	Regulator the importer works with
Nigeria	NAFDAC
Ghana	Food and Drugs Authority (FDA Ghana)
Kenya	Pharmacy and Poisons Board (PPB)
Uganda	National Drug Authority (NDA)
South Africa	SAHPRA
Egypt	Egyptian Drug Authority (EDA)
United Arab Emirates	Ministry of Health (MOH UAE)
Saudi Arabia	Saudi Food and Drug Authority (SFDA)

Planning for heat and long transit routes

Many destination markets in Africa and the Gulf involve high ambient temperatures and multi-leg routes. GPD packs temperature-sensitive products in validated packaging and includes calibrated monitoring devices where required. The monitoring data travels with the consignment, so the importer can check conditions from dispatch to arrival.

How buyers use GPD for international orders

A licensed importer in a Gulf market

The importer is sourcing temperature-sensitive products from the UK and shares its destination requirements. GPD prepares the consignment with validated packaging, monitoring devices and a documentation set aligned with what the importer submits to its regulator.

An NGO procurement team across several African markets

The team works with donor-funded health initiatives and needs one documentation standard across several markets. GPD prepares each consignment to the same GDP standard and coordinates with the authorised importer in each market.

Market-specific detail is on GPD’s regional market pages and in the procurement guide for exports to Qatar.

Frequently asked questions

What does a global pharmaceutical distributor like GPD do?

GPD is an MHRA-licensed pharmaceutical wholesaler and exporter that coordinates international pharmaceutical distribution from the UK. It prepares export-ready consignments with full documentation and hands them over to authorised importers in destination markets.

How is international pharmaceutical distribution from the UK regulated?

On the UK side, GPD exports under its MHRA Wholesale Dealer Authorisation (Human) and Good Distribution Practice. In the destination country, the authorised importer manages regulatory clearance with its national regulator.

Who uses GPD as a global pharmaceutical distributor?

Authorised importers, licensed healthcare distributors, NGO procurement teams and health ministry buyers use GPD to source medicines from the UK for international markets.

What does the authorised importer receive with each export consignment?

The importer receives certificates of analysis, batch traceability records, temperature monitoring data and export documentation aligned with the requirements of its national regulator.

Can GPD export medicines to a country where it has no local office?

Yes. GPD does not hold local representation in destination countries. It coordinates with the buyer’s authorised importer, who manages regulatory clearance and national distribution.

Discuss an export order

Tell us the products, quantities and destination market. Include your authorised importer if you have one. GPD’s team will set out the export documentation that market needs.

Discuss an export order