Following a thorough inspection by the competent health authority, we at DESTILERÍAS MUÑOZ GÁLVEZ, S.A. have renewed our Good Manufacturing Practices (GMP) certificate according to the European Directive 2001/83/CE, highlighting our dedication to maintaining the highest standards.

On this occasion, we have been able to extend this GMP certification to two new Active Pharmaceutical Ingredients (APIs) for human use.  This will allow DESTILERÍAS MUÑOZ GÁLVEZ, S.A. to increase the number of collaborations with companies in the pharmaceutical sector and 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. This meticulous documentation process ensures that all regulatory requirements are met, facilitating the approval and distribution of essential medicines.

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. Our commitment to quality and safety underpins every aspect of our operations, driving us to continually improve and innovate.