Importers: send your product list or tender and get verified manufacturers, indicative prices and document status within 48 hours. Manufacturers: list your products, dossiers and partnership needs, and see live importer demand.
Send your product list or tender. Within 48 hours you get matched GMP manufacturers, indicative prices and CoPP, GMP and dossier status for your country.
Send your list →Export finished products and APIs, out-license dossiers, find distributors, or fill contract-manufacturing capacity. List once and see live importer demand.
List your assets →Doctor or hospital? Named-patient access·Patient or family? Request a medicine
Search 3,000+ finished formulations and APIs across 66 therapeutic segments. Not in the catalogue? Send it to us and we come back within 48 hours.
Real, dated importer demand on one side; manufacturers' products, dossiers and partnership needs on the other. Demand pulls manufacturers in; their listings pull importers and partners in.
Tell us the product, market and volume, or upload your product list or tender. We structure it, match it to manufacturers with the right approvals and dossiers, and come back within 48 hours.
Global pharma trade stalls on trust — a buyer and a supplier who've never met. These make a first deal with a stranger safe.
We check the manufacturer's GMP certificate, CoPP and dossier status, and share them with you before you place an order.
Due diligenceEscrow or LC-backed payment can be arranged, depending on buyer credentials, deal size and product, so a first deal with a new partner is protected.
PaymentsEvery requirement is handled by our BD team, led by Mitul Agarwal (B.Pharm, MBA), not by an automated marketplace.
ExperienceBrand owners find a manufacturing partner; CDMOs fill idle capacity. From formulation and dossier development through to commercial supply.
Post your project — molecule, dosage form, volume, target market — and get matched to EU-GMP / USFDA CDMOs able to deliver it.
For brand ownersCDMOs publish dosage forms, certifications and available line capacity — turning idle capacity into booked orders.
For CDMOsFormulation, analytical, stability, tech transfer and CTD / ACTD dossier development — the full path to a filed, launch-ready product.
DevelopmentOriginal articles on sourcing, registration and global markets.
Describe your requirement — product, strength, destination market, volume — via the structured form, PharmaTradz AI or WhatsApp. We match it to verified suppliers with the right certifications and dossiers, and quotes come back to you in one place. If a product isn't in the catalogue, send an RFP and our team will revert with sourcing options.
We check each manufacturer's GMP certificate, CoPP and registration documents before quoting, and share them with you before you commit.
EU-CTD is the European Common Technical Document format; ACTD is the ASEAN format used across Southeast Asia. Product listings state available formats (CTD, EU-CTD, ACTD) and bioequivalence status, and many dossiers are available for out-licensing.
Yes — via our named-patient import programmes. Supply requires a valid prescription and treating-doctor details, and is handled as a clinical intake, separate from trade.
Narcotic drugs and controlled substances are supplied strictly against valid import and export permits issued by the respective competent authorities.