Officers and regulatory representatives of Documedica Italia Srl
BOTTA Martina
(a) the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released;
(b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date;
(c) the post-market surveillance obligations are fulfilled;
(d) the reporting obligations are fulfilled.