- CTD / ACTD document checklist
- Country-specific gap review
- Artwork and labelling brief
- Manufacturer evidence request
Considered sourcing. Clearer pathways.
A pharmaceutical sourcing platform for importers, distributors and institutional buyers. Explore six product lines and start with your market’s requirements.
Portfolio at a glance
An organised starting point for your next enquiry.
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- Business model
- B2B wholesale & export
- Documentation
- Product & market specific
- Credential status
- Awaiting verification
WHO-GMP evidenceSchedule M scopeISO certificationWholesale authorisationFSSAI scopeIEC registration
Less complexity. More clarity.
Sourcing pharmaceutical products is about more than finding a formulation. It means aligning the product, the manufacturer, the paperwork and the destination.
This platform brings those conversations into one place. Built for import licence holders, pharmaceutical distributors and institutional procurement teams—not direct-to-consumer purchases.
Start with a product list. Define the documentation. Establish a clear, evidence-led route to the next decision.
Our approach to sourcingSix lines. One considered portfolio.
From finished formulations to everyday healthcare. Explore the category that fits your procurement brief.
Beyond the product. Into the details.
A structured discussion of everything between the sourcing brief and a documented shipment.
Private label & contract manufacturing
Your portfolio. A clearly defined manufacturing brief.
Explore our services- Product and packaging brief
- Facility qualification checklist
- Artwork approval workflow
- Product-specific MOQ review
Bulk & institutional supply
Procurement structured around the tender, not just the product.
Explore our services- Tender specification review
- Product schedule
- Document responsibility matrix
- Delivery requirement brief
- Commercial document checklist
- Packing and marking instructions
- Origin documentation review
- Freight coordination brief
Temperature-controlled logistics
Temperature requirements belong in the first conversation.
Explore our services- Product temperature specification
- Shipping-lane risk review
- Data logger requirement
- Excursion response plan
- CoA and specification review
- Pre-shipment sampling brief
- Batch traceability checklist
- Retention-sample arrangements
Different markets. A shared discipline.
Every destination brings its own requirements. Start with the local registration pathway, then build the sourcing brief around it.
Explore regional requirementsNigeriaKenyaGhanaTanzaniaUgandaEthiopiaZambiaIvory CoastCameroonSenegalMozambiqueRwanda
Documentation planningUzbekistanKazakhstanKyrgyzstanTajikistanAzerbaijanGeorgiaArmeniaBelarus
Documentation planningVietnamPhilippinesCambodiaMyanmarSri LankaNepalBangladesh
Documentation planningPeruBoliviaEcuadorGuatemalaDominican RepublicParaguay
Documentation planningA clear next step. At every stage.
Define the product, presentation, quantity and destination.
Before we begin.
More questions? Get in touchMOQ depends on the formulation, pack size, manufacturer and whether the product is a stock or production order. Share your product list and quantities for a specific assessment.
Lead time depends on stock allocation, manufacturing, artwork approval and document readiness. A written schedule should be agreed after the product and destination review; this preview makes no delivery commitment.
Letters of credit (LC) and telegraphic transfers (TT) can be included in an enquiry. Availability, payment milestones and banking requirements must be agreed in the written quotation. No rates are published.
A typical review includes a batch CoA, invoice, packing list, certificate of origin and shipping documents. GMP evidence, Free Sale Certificates, MSDS and stability information depend on the product and destination. Confirm the complete list before ordering.
Include the product, presentation, quantity and destination in your request. Sample availability, charges, transport and import permissions require confirmation; prescription samples are not exempt from applicable rules.
Submit a product brief with proposed artwork, pack size and target country. Manufacturing scope, brand rights, MOQ, lead time and destination labelling requirements must be assessed before a private-label order.
Your next sourcing brief starts here.
Tell us what you need, where it needs to go, and the documentation your market requires. A better enquiry begins with the right details.