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Frazer-Nash approved to medical device quality standard, ISO 13485

09/07/2021
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Technology solution provider, Frazer-Nash Consultancy, has achieved certification to quality standard ISO 13485.

Technology solution provider, Frazer-Nash Consultancy, has achieved certification to quality standard ISO 13485, enabling it to better help its medical technology clients to achieve their goals.

Certification body Lloyd’s Register recommended the systems, engineering and technology company for approval against ISO 13485:2016, for demonstrating that its quality management processes and practices met the stringent regulatory requirements of the medical sector.

Celebrating the achievement, Business Manager, Martin Concannon, said:

“Medical technologies – MedTech – continue to evolve, enabling innovative solutions in the delivery of healthcare. The way in which healthcare is delivered will continue to change significantly, as a greater number of smarter, more connected devices help both health professionals and individuals manage illness. With an established track record of delivering medical device and equipment projects, from initial concept through to design for manufacture, we chose to seek ISO 13485 approval to show that our best practice processes met the highest quality management standards required for the medical industry.

“Two of our core values are ‘we care’ and ‘we do things that matter’. With the increasing health needs of the ageing population and, particularly in the current pandemic, people’s health matters more than ever – we care about making society’s health the best it can possibly be.

“I’d like to thank all the team at Frazer-Nash involved in achieving this approval – it was very much a collaborative effort – which will allow us to enhance and extend the support we offer to clients in this area, enabling them to create and develop the health-sustaining tools and equipment that make lives better.”

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