We are delighted to announce completion of our ISO 13485:2016 certification process.
ISO 13485 is a globally recognised standard, published by the International Standards Organization (ISO), setting out the requirements for quality management systems for diagnostics and medical devices. The ISO quality standard is awarded to manufacturers who demonstrate excellence in quality management and best practice for design, manufacture or supply and hence meeting the regulatory requirements specific to the IVD industry.
Fast MDx Ltd. is a molecular diagnostics company focussed on development of medical diagnostics for faster and more accurate diagnosis in healthcare, announced it has completed the quality management ISO 13485:2016 certification audit for the design and development and manufacture of molecular diagnostic platforms for infectious diseases.
The completion of the ISO 13485:2016 certification audit exemplifies Fast MDx’s commitment to meeting the highest standards of quality, reliability and safety in the medical device industry.
“ We are very proud to receive the ISO 13485:2016 certification; this achievement demonstrates our continuous commitment to consistently high standards in our quest to deliver the Fast MDx platform.” said Richard Lewis, CEO.
“Fast MDx are focussed on delivering the world’s first, low-cost, high-throughput, near-patient molecular diagnostic test system, and our ISO accreditation is another successful step in the journey.”