The Importation Pipeline
We manage each step meticulously to preserve medical efficacy and guarantee legal regulatory compliance.
WHO-GMP Manufacturer Auditing & Sourcing
Before placing any corporate purchase orders, our procurement experts vigorously verify the manufacturing facility's WHO-GMP (World Health Organization - Good Manufacturing Practices) certifications. We perform exhaustive clinical audit documentation checks, examining European, Asian, and American production sites to guarantee compliance with the highest international pharmaceutical standardizations.
NAFDAC Import Permits & Dossier Filing
We manage the end-to-end regulatory bureaucracy by filing all required pharmaceutical datasets with NAFDAC (National Agency for Food and Drug Administration and Control) and the PCN. By securing the critical importation permits prior to shipment, we ensure every therapeutic product entering Nigeria possesses legally verified national registration codes.
Pre-Shipment Batch CoA Quality Testing
Once a batch is manufactured at the source, we mandate independent chemical checks of the Certificate of Analysis (CoA) against global pharmacopoeia benchmarks (USP/BP/Ph. Eur.). This proactive validation isolates formulation errors and actively prevents substandard, diluted, or counterfeit compounds from being boarded onto shipping carriers.
Secure Transit & Rapid Lagos Customs Clearance
Utilizing medically qualified air and sea cargo carriers, temperature-sensitive items are shipped directly to major Lagos hubs. Our dedicated customs clearing specialists execute rapid-release procedures at the ports to avoid prolonged storage exposure. Sensitive cold-chain biologics and generic antibiotics are then routed immediately to our climate-controlled Ilupeju distribution depots.