WHO-GMP pathway assessment
Review GMP status, dossier gaps, CoA evidence, and destination requirements before regulated trade.
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See which companies in each country are licensed to buy or supply your product, and the certifications they hold.
Complete four gates and earn your Blue Tick. Your regulator-issued licence is checked.
Search products and companies across the global healthcare directory.
See which companies in your target countries are licensed for your product, and the certifications they hold.
Ask PMX AgentMessage matched companies and send your RFQs to them directly.
You negotiate and close with each other. PMX stays out of the deal.
Ask in plain language who makes or supplies a product in the markets PMX covers. Answers come from regulator registers and PMX member profiles, with each company's licence status and certifications alongside.
Browse products by category, from finished medicines to APIs and biologics.
Choose your member type. Every member completes the same four gates to earn a Blue Tick.
Upload the documents you already have: PMX reads them and fills in the details, and a product catalogue PDF fills in your product listings.
Who you are, where you operate and your regulator-issued licence number.
Upload the licence and certificates your company holds.
Sellers list the products they sell; buyers set out what they source.
Your membership starts and your Blue Tick is issued.
The member’s regulator-issued licence has been checked, and the member has declared responsibility for the authenticity of its information at every gate.
Buyers and sellers negotiate and contract with each other.
One yearly subscription. PMX takes no share of your business.
Arrange payment and logistics between yourselves, the way you already do.
Supplier and buyer workflows are checked against country-specific regulatory requirements. WHO-GMP, SFDA, NMPA, DRAP, and other credentials are validated where applicable.
Every supplier has a real-time Composite Quality Score based on batch data, deviations, CoA accuracy, and delivery performance.
Built-in regulatory pathway guidance for WHO Prequalification, SFDA, NMPA, and EMA. Compliance documentation generated automatically.
Country-specific workflows for supplier readiness, raw-material import, and export documentation.
Review GMP status, dossier gaps, CoA evidence, and destination requirements before regulated trade.
Learn MoreA stage-by-stage import workflow: supplier documents, DRAP clearance, port testing, and post-market obligations for active ingredients and raw materials from any origin.
Learn MoreGenerate Certificates of Pharmaceutical Product (CoPP), GMP certificates, and Free Sale documents, matched to each destination market’s requirements.
Learn MoreThe pharmaceutical manufacturing sector spans established generic and branded medicine producers serving regulated and growth markets across the Middle East, Africa, Central Asia, and Southeast Asia. Demand for affordable, quality-assured medicines continues to grow as buyers seek competitive pricing, reliable supply, and verifiable quality standards.
Despite this growth, the sector faces persistent challenges in international markets and raw-material sourcing: inconsistent regulatory compliance documentation, fragmented quality assurance systems, difficulty navigating country-specific requirements (WHO-GMP, SFDA, NMPA, EMA, DRAP), and limited transparent pricing mechanisms. Buyers and importers often struggle to verify supplier credentials, batch quality data, API documentation, and shipment eligibility.
PMX Pharma Exchange bridges these gaps with a compliance-linked exchange: members’ licences are checked, suppliers maintain a real-time Composite Quality Score (CQS), and buyers and sellers deal with each other directly. By combining regulatory technology with B2B commerce, PMX enables pharmaceutical buyers and suppliers to trade with verifiable quality credentials.
Common questions about pharmaceutical sourcing on PMX
Complete the four gates and subscribe to join the exchange.