Alven’s QA/QC team is focused on all activities with any potential influence on the product quality, on the environment and the health and competences of our employees, and undertakes to control them. All with the aim of constant improvements.

Our quality system is based on the Czech Act on Pharmaceuticals, the Decree on Good Manufacturing Practice and other guidelines and directives published by the Czech State Institute for Drug Control (SUKL) and European and international authorities.

State-of-Art equipped laboratories and experienced quality control staff ensure the production monitoring at every technological stage. Development, validation and transfer of analytical methods are performed in co-operation with universities and state accredited laboratories.

Our QA personal is experienced in authority inspections as the SUKL, FDA, EDQM, etc. Dossiers on our active pharmaceutical ingredients are prepared for registrations in any territory.