Last week, NEOS underwent its annual quality management system audit by TÜV SÜD. This year’s audit was focused not only in achieving the recertification of our quality system under the ISO 13485 standard, but also in demonstrating its alignment with the requirements of the Medical Devices Regulation in Europe.

During these four days, we had the opportunity of presenting in detail how we work to develop and commercialize medical devices that aim at improving the patients’ quality of life by complying with the relevant regulatory and legal requirements, as well as the technical standards defining the state of the art in the fields of Neurosurgery and Cardiothoracic surgery.

We thank the auditors at TÜV SÜD for their insightful evaluation and for providing the opportunity of identifying ways to improve our daily work, and we are also grateful to all of NEOS’ personnel for their commitment in achieving the company’s goals.