With 80 years of experience, UQUIFA’S business model is based on a combination of a quality manufacturing platform and a track record of service and reliability. UQUIFA is a manufacturer of Active Pharmaceutical Ingredients (APIs) and intermediates for the pharmaceutical and animal health industries globally. The Company has 4 manufacturing sites (2 in Spain, 1 in Hungary and 1 in Mexico) with strict adherence to all regulatory norms. These sites operate under cGMP conditions and have been inspected and approved by global pharmaceutical companies and leading regulatory authorities.


All UQUIFA's sites operate under cGMP conditions and have been inspected and approved by the FDA, EDQM, ANVISA and/or KFDA.

UQUIFA has pilot plants al all three facilities in Spain and Mexico. These plants are located on FDA approved sites and the pilot plants in particular have been inspected and approved by the FDA for small scale API/NCE production. Dedicated qualified technicians run the plants under cGMP guidelines and using identical quality control systems to those used for commercial production.

The Spanish R&D Laboratory is located at Sant Celoni (50 km North from Barcelona, Catalonia). The 800 square meters building holds the Synthesis and Analytical development laboratories.

Reduction of batch production time and the elimination of toxic and dangerous reagents is our life blood at Uquifa.


Uquifa S.A.U.

Barcelona C/ Mallorca 262, 3rd floor

Barcelona, 08008


Phone: (908) 335 4990

Contact: Frank Derrien


  • Find out about Uquifa’s service offering and what makes this company uniquely positioned to support customers in the outsourcing of small molecule APIs.