After inspection by the competent health authority, we have renewed our Good Manufacturing Practices (GMP) certificate according to the European Directive 2001/83/CE.

On this occasion, we have been able to extend this certification to two new Active Pharmaceutical Ingredients (APIs) for human use, which will allow us to increase the number of collaborations with companies in the pharmaceutical sector to contribute to the elaboration of effective and safe medicines endorsed by GMP regulation through the registration of Active Ingredients before the corresponding Drug Agencies.

DMG will prepare and register ASDMF (Active Substance Drug Master File) documents to be later used by its customers in the registration of the final medicine for human use.

Through the implementation and maintenance of international pharmaceutical Quality standards, DESTILERÍAS MUÑOZ GÁLVEZ, S.A. seeks to meet the needs of our customers and society to have effective and safe medicines for human use.