Large commercial scale batches are produced at UQUIFA’s main manufacturing plants after validation runs have been completed.
Regardless of the age of a process, a multi-discipline team regularly meets to discuss continued cost reduction and quality improvement.
UQUIFA's manufacturing sites operate under cGMP conditions and have been successfully inspected by the FDA, other national agencies and by major pharmaceutical companies.
Safety and environmental compliance are our highest priority and the sites have ISO 14001 certification as well as European cGMP certificates. Our Project Management System and our Regulatory Team supports the project through scale up and onto mainstream manufacture.