API & Medical Consumables Sourcing

Active pharmaceutical ingredients, excipients, medical consumables and pharmaceutical packaging sourced from Chinese manufacturers for export.

We provide international trade and business docking services for pharmaceutical and life-science products, from a single API enquiry through to a repeat supply arrangement.

Product Scope  

  1. Active Pharmaceutical Ingredients & Intermediates: APIs and key starting materials, with the compendial standard stated on the enquiry — USP, EP, JP or ChP — so the grade is fixed before a quotation is issued.
  2. Excipients & Finished Preparations: Pharmaceutical excipients, and finished preparations where the destination market permits import.
  3. Medical Consumables & Devices: Single-use consumables and related medical supplies.
  4. Pharmaceutical Packaging Materials: Primary and secondary packaging — glass and plastic containers, closures, blister and foil materials.

Documentation & Compliance Support  

Which documents a buyer needs depends on the destination and the product, so we establish that at the enquiry stage rather than after shipment. We assist with:

  • Manufacturer documentation — certificates of analysis, specification sheets, and the manufacturer’s GMP status and audit history
  • Regulatory filing routes, including US FDA drug master files and European CEP / ASMF submissions held by the manufacturer
  • SDS and transport classification for products that ship as dangerous goods
  • Certificates of origin and the consular or legalised documents some markets require

We do not hold the manufacturer’s regulatory filings ourselves; we identify which manufacturer holds what, and obtain it in writing before a quotation goes out.

Technical Services  

Pharmaceutical technology consulting, technology transfer support, and compliance-path assistance for health-industry projects entering or leaving China.

What to Include in an Enquiry  

A complete enquiry is normally quoted within one business day:

  • Product name, CAS number and compendial standard (USP / EP / JP / ChP)
  • Annual volume or batch quantity, and whether the material is for R&D, clinical or commercial use
  • Destination country and the regulatory route the buyer intends to use
  • Packaging requirement and destination port, with Incoterms
  • Which documents are required — CoA, GMP certificate, DMF or CEP reference letter, stability data