We are mad at software production for medicine. We want to be the best in what we do so we produce, implement and maintain “Quality Management System” that meet the requirements of EN ISO 13485 and EN ISO 9001 norms as well as the “Act on Medical devices” and 93/42/EEC directives.
- monitor quality of our products,
- train our staff in terms of law regulation changes and new solutions,
- react on every adverse effects, providing necessary resources we will make every effort to improve the system.