To design, implement and maintain a Quality System meeting the cGMP requirements as defined in the European Directive for the manufacture of finished pharmaceutical products.
To meet the needs of doctors and patients related to our services and products.
To continually improve, to plan, produce and monitor our products in order to minimize environmental effects in production and usage stage.
We are responsible to ensure manufacturing of medicinal products that:
Feel ethic rules
Fit their intended purpose
Comply with the requirements of the marketing authorisation.
Do not place patients at risk due to inadequate safety, quality or efficacy.
We are also committed to:
Continual improvement, in order to reduce the environmental impacts and to prevent environmental pollution.
Optimization of raw materials consumption in order to save natural resources.