Dirigeants et représentants réglementaires de TERUMEDICAL
BERECHET COMANESCU Petre
Checking the conformity of the devices in accordance with the quality management system (QMS) before release of the product n the market.
Preparing and maintaining the technical documentation end EU Declaration of Conformity - Meeting post market surveillance obligations. - Vigilance reporting and analysis requirements are met, including serious incidents field, safety corrective actions and report trending. For investigational devices a signed statements that the device meets the GSPRs.