All medical
devices are CE-labelled and manufactured under strict compliance
with applicable national and international standards and regulations.
Production of medicinal products is carried out according to European
GMP standards. All medicinal products and medical devices are released
only after passing through strict in-process and final quality controls.
Furthermore,
PRO-MED AG assures the quality of our products by employing only
qualified suppliers for raw materials and releasing raw materials
for production only after stringent incoming controls. |