Sechrist Industries Inc

Check the conformity of devices in accordance with the QMS under which the device is manufactured before the device is released into the EU market. Ensure the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date in accordance with the EU MDR. Ensure the post-market surveillance obligations are complied with in accordance with the EU MDR. Ensure the reporting of serious incidents and field safety corrective actions are in accordance with the EU MDR.

Check the conformity of devices in accordance with the quality management system under which the device is manufactured before the device is released into the EU market. Ensure the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date in accordance with the EU MDR. Ensure the appropriate statement is issued in accordance with the EU MDR in case of investigational devices.

Check the conformity of devices in accordance with the QMS under which the device is manufactured before the device is released into the EU market. Ensure: the technical documentation and the EU declaration of conformity are in accordance with MDR, post-market surveillance obligations are complied with in accordance with MDR, reporting of serious incidents and FSCAs are in accordance with MDR, appropriate statement is issued in accordance with MDR in case of investigational devices.