SWISS COMMERCIAL COORDINATION · INTERNATIONAL MANUFACTURING CONNECTIONS
APIs & PHARMACEUTICAL INTERMEDIATES
Manufacturing & quality

A transparent view of the manufacturing partner.

Manufacturing information below is reported in the partner’s supplied manual. These facilities are in China and are not owned by Vadawiss.

01

Facilities in China

Our Manufacturing Partner is located in Xi’an, Shaanxi, China. Its manual reports a facility area of 14,000 m².

02

Development & production equipment

The manual depicts an R&D laboratory, quality-testing equipment and production equipment labeled 100 kg and 1,000 kg. These labels are not annual capacity commitments.

03

Quality management

The partner’s manual states that its facilities follow cGMP requirements and that its quality system is established in accordance with China GMP regulations and ICH Q7 guidelines.

Qualification is project-specific.

Manual statements are manufacturer-reported information, not independent verification or a claim of regulatory approval. No GMP certificate or market authorization is asserted by this website.

Discuss the evidence you need

  • Agreed product specifications and analytical methods
  • Batch-specific certificate of analysis
  • Safety data and handling information
  • Applicable quality-system evidence
  • Audit or supplier-qualification requirements

Documentation availability and suitability require confirmation with Our Manufacturing Partner.

Let’s align on your quality requirements.

Share your target material, specification, quantity and timeline with our Swiss coordination team.

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