Our Expertise

Clinical Trial Support & Import Coordination

We handle the full lifecycle of pharmaceutical market entry and operations across Africa and Asia-Pacific.

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Clinical Trial Support & Import Coordination

PharmaMED Solution Limited provides end-to-end clinical trial supply and logistics support across African markets, helping sponsors and Contract Research Organisations (CROs) source, import, distribute and manage investigational medicinal products (IMPs) and other .

Our services include:

1: Innovator Sourcing & Procurement
Sourcing genuine innovator medicines, reference-listed products, comparator drugs and other trial-specific products through appropriate supplier channels, in line with study requirements.

2: IMP Import Coordination & Customs Clearance
Coordinating import permits, regulatory documentation, shipment clearance and cross-border movement of clinical trial supplies.

3: Inventory & Distribution Management
Tracking stock levels, batch numbers, expiry dates, shipment movements and product allocation across trial sites.

4 : Cold-Chain Logistics
Coordinating temperature-controlled storage, transportation, monitoring and documentation to maintain product integrity where required.

5 : Reverse Logistics & Product Reconciliation
Coordinating the collection, return, reconciliation and authorised disposition of unused, expired or returned investigational medicinal products (IMPs), in accordance with applicable regulatory requirements and sponsor procedures.

From innovator sourcing and procurement to site delivery and study close-out, we help streamline clinical trial supply chains through coordinated logistics, product traceability and regulatory compliance support.

From innovator sourcing and procurement to site delivery and study close-out, we help streamline clinical trial supply chains through coordinated logistics, product traceability and regulatory compliance support.

What happened: A multinational CRO needed to move IMP for a Phase 3 trial across three East African sites within 72 hours of regulatory approval. We processed customs clearance in Nairobi (24 hours), Kampala (36 hours), and Dar es Salaam (48 hours). Trial enrolled on schedule with zero regulatory or logistics delays.
Best for: Global sponsors running trials across East Africa, CROs that need reliable logistics partners in-country, and anyone who can't afford delays because trial timelines are fixed and enrollment windows are narrow.
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