CHAN Medi-Pharm operates a specialized, highly regulated medical supply chain network, powered by cold-chain integrity, advanced tracking, and a specialized fleet.
Structured around three critical pillars to support major public health initiatives and donor-funded projects.
Heavy-duty, multi-axle freight trucks connecting central ports and donor hubs directly to regional distribution centers (Jos, Numan, Owerri). Features bulk cross-docking for anti-malarials and vaccines.
Pharma-grade vans and 4WD vehicles optimized for rough terrain. Equipped with active refrigeration and passive cooler boxes for strict 2°C to 8°C cold chain compliance.
Fast-tracked collection for batch recalls, expired commodity management, and retrieval of reusable cold-chain equipment (data loggers, pallets).
Managing a nationwide storage footprint of 15,000 cubic metres optimized for pharmaceuticals.
Dual large-scale Cold Room units at Jos and Owerri hubs for thermo-labile products (vaccines, blood products). All depots feature medical-grade refrigerators with digital data loggers.
Strict NAFDAC regulations. Every depot is managed by Qualified Pharmacists ensuring batch tracing, expiration management, and Rational Use of Medicines.
A sustainable service operating across 400+ Member Institutions and 4,000 affiliated clinics.
Acting as a strategic aggregator bridging global manufacturers and frontline facilities.
Pooling inventory of 400+ hospitals to secure factory-gate pricing. Sourcing is restricted to WHO-cGMP compliant and NAFDAC-registered manufacturers to eliminate counterfeits.
Cost-recovery model stabilizes prices in rural areas. We maintain inventory buffers in conflict-affected zones to guarantee equity of access regardless of location.
Targeting key building blocks of the health system to create systemic resilience and permanent institutional capacity.
A frontline defense against Substandard and Falsified (SF) medicines, operated by qualified pharmacists at the central Jos hub.
Examining packaging, batch labels, font uniformity, and physical tablet characteristics against reference standards.
Testing how fast a tablet breaks down in water at body temperature (must be 15-30 mins, else API cannot be absorbed).
Fast chemical tests confirming the correct active drug class is present, revealing inert fillers.
Isolates the compound to assess Identity, Content/Potency (detects under-dosing), and Impurities.
If a sample fails, the batch is immediately quarantined in the digital warehouse system. It is then escalated to WHO-prequalified confirmatory labs (like MEDS Lab or Difaem), and data is reported to NAFDAC and WHO rapid alert systems.