RÖS'S renews its prestigious certification ISO 13485:2016 for medical device quality management systems. This certification demonstrates the commitment continuous from the company with the quality and the excellence in all its products and services.
The ISO 13485:2016 standard establishes the requirements for a quality management system specifically designed for organizations that manufacture or supply medical devices. With this certification, RÖS'S demonstrates its ability to meet the most rigorous international standards in terms of quality, safety, and regulatory compliance.
The ISO 13485:2016 certification reinforces RÖS'S ESTÉTICA's position as a Reliable supplier of medical and aesthetic devicesensuring that its manufacturing processes and procedures meet the highest standards high standards of quality and safety.
As part of RÖS'S ESTÉTICA's commitment to transparency and open communication, the company is committed to maintaining ISO 13485:2016 certification through regular audits and continuous improvements in its processes and quality management systems.
