ISO–13485 Re-Certification
Published: 27 September 2021
We are very proud to announce our continued certification to the Medical Devices international standard ISO-13485 – an accreditation we have held with distinction for 14 years.
Successful independent evaluation to this standard, including regulatory requirements for devices, underlines our full commitment and core objectives in pursuit of the highest Customer and employee satisfaction.
Quality Manager Scott Graham commented: “Whilst a key component in the delivery of successful, robust, and regulated devices to our Customers, the ISO-13485 standard goes far beyond the scope of solely product quality. It demands that all other business elements and functions meet the exacting standards expected of the medical and pharmaceutical industry. This key milestone is testament to the teamwork and effort of the entire company and our partners.”
From this platform we can successfully deliver against our continuous improvement objectives to meet and excel in Customer requirements and support our future growth plans in the global medical sector.
Successful independent evaluation to this standard, including regulatory requirements for devices, underlines our full commitment and core objectives in pursuit of the highest Customer and employee satisfaction.
Quality Manager Scott Graham commented: “Whilst a key component in the delivery of successful, robust, and regulated devices to our Customers, the ISO-13485 standard goes far beyond the scope of solely product quality. It demands that all other business elements and functions meet the exacting standards expected of the medical and pharmaceutical industry. This key milestone is testament to the teamwork and effort of the entire company and our partners.”
From this platform we can successfully deliver against our continuous improvement objectives to meet and excel in Customer requirements and support our future growth plans in the global medical sector.
