Supplier Qualification
Screening manufacturing partners, DMF/EDMF/USDMF, CEP status and inspection history.
Sales, marketing, sourcing and distribution support for active pharmaceutical ingredients, finished formulations and CMO projects.
Screening manufacturing partners, DMF/EDMF/USDMF, CEP status and inspection history.
COA, MSDS, GMP documents, change control and technical communication.
Support from R&D stage through commercial supply and continuity review.
API BUSINESS EXPANSION is a privately owned sales and marketing company with more than 20 years of experience in marketing, sourcing, introducing and distributing active pharmaceutical ingredients and finished formulations across the MENA region.
We give API manufacturers the right regional exposure and help build long-term, transparent relationships between clients and suppliers.
Our customer-oriented team continuously expands its portfolio, connecting clients with reliable manufacturing partners and the quality documentation needed for smooth registration with health authorities.
offices in Dubai · Beijing Hong Kong · Tokyo · Melbourne Berlin · Montreal & UK
We work like an extension of your own sourcing team for API, finished-product and CMO requirements.























API sourcing with attention to DMF/EDMF/USDMF, CEP status, inspection background and regulated-market documentation.
Technical and commercial support from R&D stage through scale-up and commercial supply.
FDF and contract manufacturing coordination for selected regulated-market requirements.
Supplier communication, sample coordination, documentation follow-up and change-control awareness.
Selected manufacturing partners include sites with EU GMP, US FDA inspection history, PMDA approval or inspection experience, CN GMP and other market-specific qualifications where applicable.
Qualification status is verified by product, site and project before disclosure or supply.
Send the product name, target market and requested quantity if available.
We review suitable manufacturers, qualification background and supply continuity.
Technical documents, GMP materials and regulatory support files are coordinated.
Samples, technical questions, visits and audit preparation can move forward.
Order execution, communication and change-control signals are followed up.
For an initial inquiry, please send the product name, target market and requested quantity if available. We will first check whether suitable supply options are available. Regulatory documents, samples, timeline and commercial terms can then be discussed step by step.