Officers and regulatory representatives of Overmed srl
BALOSSINO Rossella
Ensuring that 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.
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ULIVI Lorenzo
Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. Ensuring that the post-market surveillance obligations are complied with in accordance with MDR Article 10(10). Ensuring that the reporting obligations referred to in MDR Articles 87 to 91 are fulfilled. Ensuring that, in the case of investigational devices, the statement referred to in MDR Section 4.1 of Chapter II of Annex XV is issued.