Global pharma sourcing · Built for ROW
Your global pharma sourcing desk.
One partner. Every dosage form. WHO-GMP backed. ROW-ready.
We help importers, distributors and tender buyers across Africa, LATAM, MENA, CIS and Southeast Asia source compliant pharmaceuticals — with dossiers, logistics and accountability handled.
- 361
- Molecules live
- 562
- SKUs listed
- 100%
- WHO-GMP backed
- 24h
- Quote turnaround
Products are made at partner manufacturing plants; specific approvals vary by plant and market. Every partner plant is WHO-GMP certified.
01 — What we supply
Every dosage form a global buyer asks for.
Finished formulations sourced exclusively from WHO-GMP certified manufacturers, organised the way your team actually shops for them.
- TabletsImmediate-release, extended-release, chewable and dispersible.
- CapsulesHard and soft gelatin capsules across strengths.
- InjectablesVials and ampoules — liquid and lyophilised.
- SyrupsOral liquid formulations, adult and paediatric.
- SuspensionsOral suspensions for a range of therapeutic categories.
- OintmentsTopical ointments for dermatological use.
- CreamsDermatological and medicated topical creams.
- GelsTopical and applicator-based gel formulations.
- DropsEye, ear and nasal drops.
- InhalersInhalation formulations for respiratory conditions.
- PowdersOral and reconstitutable powder formulations.
- Other formulationsDosage forms outside the categories above — ask us.
02 — How a registration runs
From enquiry to a registered product.
Sourcing is the easy half. What decides whether your product reaches a shelf is the dossier — compiled to your regulator's format, defended through queries, and backed by a plant whose approvals match.
See the quality & documentation stack- 01
Enquiry
Target country, molecule, dosage form and volumes.
- 02
Plant & dossier match
A WHO-GMP plant whose approvals fit your regulator.
- 03
CTD / ACTD compile
Module-by-module compilation against the market’s format.
- 04
Country submission
Filing, queries and artwork in the required languages.
- 05
Registration & supply
Approval in hand, then repeat orders on a known lead time.
Manufacturers we source from are approved by
- WHO-GMP
- EU-GMP
- US FDA
- UK MHRA
- ISO 9001
- WHO-GDP
- NAFDAC
- ANVISA
- SFDA
Products are made at partner manufacturing plants; specific approvals vary by plant and market. Every partner plant is WHO-GMP certified.
03 — Where we deliver
Built for Rest-of-World. Compliant for every market.
Africa, LATAM, MENA, CIS and Southeast Asia — tell us your target country and we'll map the regulatory pathway, dossier needs and Incoterms before you commit.
04 — Start the conversation
Tell us your target country. We'll map the pathway.
Share your market, target product and registration status. You'll get a structured response within one business day — including dossier readiness, MOQ, lead time and Incoterm options.