(+34) 91 184 19 18 info@qilu-pharma.es

We work on the basis of the quality of our products, using the most advanced equipment and technologies with automatic production lines, instruments for analysis and control systems which are designed, installed and validated in accordance with the principles and guidelines of good manufacturing practices (GMPs) of the European Unión.

We have GMP approval from the major regulatory agencies such as USFDA (US Food and Drug Administration), EDQM (European Directorate for the Quality of Medicines) , TGA (Therapeutic Goods Administration of Australia), MHRA (Medicine and Healthcare products Regulatory Administration  United Kingdom) , MCC (Medicine Control Council Africa), MHLW (Ministry of Health, Labour and Welfare Japan) y KFDA (Korea Food and Drug Administration), successfully completing their audits.