Dirigeants et représentants réglementaires de Medicofarma S.A.
KIJEK Michał
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 reporting obligations referred to in Articles 87 to 91 are fulfilled;