Dirigeants et représentants réglementaires de Levicare
GŁĄB Wojciech
-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;
-the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date;
-the post-market surveillance obligations are complied with in accordance with Article 10(10);
-the reporting obligations referred to in Articles 87 to 91 are fulfilled;