Including an R&D perspective in our activities, taking into account the environmental impacts of our products and infrastructure.

To offer high quality products in an accessible manner by keeping customer satisfaction at the highest level.

To increase the efficiency of our production processes in line with the continuous improvement approach.

To carry out activities in compliance with national and international legal obligations, laws, ethical rules and quality standards.

Providing the necessary resources for the effective implementation and continuous improvement of our risk-based quality system.

To ensure the implementation of the “EN ISO 13485:2016/A11:2021: Medical Devices-Quality Management Systems - Requirements for regulatory purposes” standard and the “(EU) 2017/745 Medical Devices Regulation” for our services in the medical field and to develop and maintain their effectiveness.