Quality and Regulatory
Our mission is to enable low-cost, portable, 3D X-ray devices that improve the diagnosis of patients. To do this, we are developing products in accordance with ISO 13485:2016, driven by a risk focussed approach based on ISO 14971:2012.
We will comply with the relevant sections of IEC-60601-1 for our hardware; IEC 62304 for our software.
Our aim is to grow and evolve our Quality Management System to support potential customer market location requirements, including the United States (FDA), Europe (MDR 2017/745), Japan, China and South Korea.
Adaptix Limited implements and maintains an effective Quality Management System designed to enable the delivery of innovative low dose digital tomosynthesis Flat Panel X-ray medical devices and related services. We aim to ensure that we consistently exceed customer expectations and to address customer satisfaction through the effective setting of company objectives including continual improvement and the prevention of nonconformity.
The Company's directors and all staff are committed to complying with the regulatory and safety requirements applicable to medical devices and related services and to ensure the continual effectiveness of our Quality Management System.