Endocarts International Limited

1) Verify that the conformity of the devices is appropriately checked in accordance with the QMS before a device is released. 2) Maintain and update the technical documentation and declaration of conformity 3) Review complaints reportability and submit incident report to CA/AR/NB, if applicable 4) Review and compile periodic post market surveillance report (PMS) 5) Review and update the clinical evaluation report (CER)