Ghatwary Medical GMS

1. Ensuring that the conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before a device is released. 2. Ensuring that the technical documentation and the EU DOC are drawn up and kept up-to-date. 3. Ensuring that the post-market surveillance obligations are complied with. 4. Ensuring that the reporting obligations of Vigilance System are fulfilled. 5. Registration process. 6. Any other duties under article 15 of EU MDR