Officers and regulatory representatives of Levante srl
PARLATI Angela
check the conformity of the device based on the quality management system under which the devices are manufactured, before a device is released; draw up, keep up-to-date the technical documentation and the EU declaration of conformity; ensure the post-market surveillance obligations in accordance with Article 10(10); ensure the reporting obligations referred to in Articles 87 to 91; in the case of investigational devices, issue the statement referred to in Section 4.1 of Chapter II of Annex XV