Officers and regulatory representatives of Terrats Medical S.L.
ESCRIBANO Cesar
- check conformity of devices in accordance with the quality management system under which the devices are manufactured, before release. - check technical documentation and EU declaration of conformity are drawn up and kept up-to-date. – Comply with post-market surveillance obligations (according to Article 10(10)). Fulfill with reporting obligations referred to in Articles 87 to 91.