The Vitalograph design and manufacturing facility is located in Ennis, Ireland. Quality assurance extends throughout all functions at Vitalograph for greater company efficiency, reliability and improvement of product and customer service. Our processes are varied and are required to meet the requirements outlined below. For information on the standard for a particular device, please see our product pages.
The Ennis facility is accredited to EN ISO 13485, which specifies requirements for a comprehensive quality management system (QMS) applicable to the design, development, production, distribution, and servicing of medical devices.
This forms the baseline for our facility QMS, upon which we add the requirements of jurisdictional quality system regulations and associated standards. Compliance ensures our devices meet the requirements for safety and performance, from the design process through production, to patient use, and eventual device disposal.
Vitalograph’s software development process complies with the international standard IEC 62304 medical device software standard. This standard is a requirement for the development and maintenance of medical device software which includes software used on mobile devices, software intended as a standalone medical device, and software or firmware embedded within medical devices.
It is intended to cover the whole software lifecycle, from initial specification, safety classification, software development process, development process documentation, software maintenance, software risk management, configuration management and the software problem resolution process. Software development is included as a key component within the ISO 14971 process for medical devices risk management.
Risk management is a critical component of any medical device manufacturer’s QMS, and Vitalograph conform to the ISO 14971 risk management standard across all elements of the QMS, including post production activities where data is fed back into our risk process to allow us to improve both device and process as necessary.
The European Community recognized the need for standards on medical device safety and performance, and published the Medical Device Directives in 1995, laying down mandatory requirements for product safety and performance, with guidelines for ensuring safety even when no particular standards existed. Conformance to the requirements to permit the placement of the CE Marking on our devices is overseen by our Notified Body, BSI (2797), and by the Health Products Regulatory Authority (HPRA) in Ireland.
The new European Medical Devices Regulation 2017/745/EC, the MDR, will replace the Medical Devices Directive (93/42/EEC), the MDD, in May 2021 including a three year transition period. Vitalograph is working with our Notified Body and the HPRA to transition our QMS and our devices from CE Marking under MDD to CE Marking under MDR during this transition period.
In 2019 Vitalograph received its Medical Device Single Audit Program (MDSAP) Certificate, following rigorous audits in our Ennis facility. The MDSAP program centres on adherence to the quality system regulations from each of the participating MDSAP countries. It provides a means by which medical device manufacturers can have a single audit program by designated 3rd party Auditors to prove compliance with the regulatory requirements of these countries.
Vitalograph’s QMS, device design and production are audited under MDSAP Program against the QSRs of The United States of America, Australia, Brazil, Canada, and Japan.