Committed to Quality and Reliability
“The ISO 13485:2016 standard provides dpiX with the requirements for a comprehensive quality management system in the design and manufacture of medical devices, helping the company establish and maintain quality products and product realization. It also fosters dpiX’s ability to meet customer requirements in the production of medical components.” – Byung Park, Vice President of Engineering.
In early 2003, dpiX selected the ISO 9001:2000 standard as the foundation on which to build a comprehensive Quality Management System (QMS). Seven months after dpiX embarked on its quest to achieve ISO 9001:2000 registration, dpiX became a registered ISO company. dpiX successfully made a rapid transition from a predominately research and design-focused company to one dedicated to high volume, innovative design, and efficient manufacturing that puts customers and quality first. Continuing its commitment to quality over the years, dpiX gained registration on all ensuing 9001 updates, and in 2018, obtained certification on the ISO 13485:2016 standard to address dpiX’s role in the manufacture of medical devices.
Through the application of the dpiX Quality Policy, full compliance with ISO required QMS procedures, and continuous management review, dpiX continues to lead the way for the successful design, development, and manufacturing of quality a-Si sensor arrays.
dpiX Environmental Policy
“dpiX is committed to reducing our impact on the environment.” – Frank Caris, President & CEO
On July 29, 2004, dpiX received ISO 14001 certification. In addition to preventing pollution and complying with environmental regulations, dpiX strives continuously to improve our Environmental Management System. In 2017, dpiX earned registration on ISO 14001:2015, the latest version of the standard. dpiX has been a Gold Leader within the Colorado Environmental Leadership Program since 2011. dpiX can provide product compliance declarations for the applicable requirements of REACH, RoHS, and Conflict Minerals.