Dipharma SA has developed a Quality Management System in line with the international requirements for cGMP, GDP, GCP and GVP.
Dipharma SA ensures that all activities outsourced to external providers (e.g. CMOs, CROs) are carried out by experienced, qualified, state-of-the–art, Health agency certified centres.
Every provider is selected on the basis of specific quality evaluations and quality audits carried out by our internal QA Department. Dipharma SA has implemented a yearly audit plan for internal procedures and for all external providers.



Safety and Quality are Dipharma’s core values and, every day, skilled professionals work in our
European facilities to produce high quality and safe active pharmaceutical ingredients (APIs).
For more than 60 years our passion and commitment have been to achieve the highest levels of quality and customer satisfaction, together with innovative solutions. For this reason, Dipharma Group, with more than 200 patent applications filed, devotes substantial attention and resources to ensure continuous improvement in its production processes and to develop a strong quality culture, a guarantee for the health and safety of patients taking Dipharma active pharmaceutical ingredients.