PharmaTradz is a global B2B pharmaceutical sourcing partner for finished dosage forms — our core strength — and APIs across every therapeutic segment. Tell us what you need and we identify the right manufacturer, handle the documentation and come back with quotes. Tell us who you are:
Importer / distributor seeking finished formulations and APIs in bulk.
TradeManufacturer or CMO wanting qualified demand & white-label leads.
TradeNamed-patient access, compassionate use or institutional supply.
ClinicalPatient / caregiver seeking an unavailable or unaffordable drug.
ClinicalFinished formulations first, plus APIs, intermediates and devices. Search, filter and send a structured RFQ in a click.
Updated monthly from live RFQ data — see the full Demand Index →
Tell us the product, market and volume — we structure it, match it to verified suppliers and ready dossiers, and your quote comes back. No more free-text guesswork.
Real dated buyer demand on one side, dossiers ready for licensing on the other. Demand pulls suppliers in; available dossiers pull buyers and licensees in.
Global pharma trade stalls on trust — a buyer and a supplier who've never met. These make a first deal with a stranger safe.
KYC business checks, verified GMP certificates and export history — a Verified mark on every profile so both sides know who they're dealing with.
TrustBuilt-in verification systems and structured documentation ensure secure, compliant dealings on first deals with new partners.
PaymentsCompleted-deal count, response time and ratings. Reputation that accrues and rewards the reliable partners on both sides.
ReputationWe're collecting reviews from our verified buyers and suppliers — be the first to share your experience.
Brand 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.
Every supplier passes KYC business checks; GMP certificates and export history are verified before the Verified mark appears on a profile.
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.
Online · B2B Pharma Sourcing · NPP