Founded in 2000 Medical Device Management was established with the aim of assisting medical device companies to bring their products to market by helping these companies navigate the requirements of legislation such as the Medical Device Directive.
Over the years we have worked with dozens of companies many of whom we work with to this day. We focus on building long term relationships with our clients helping them to face the evolving challenges of regulations such as the Medical Device Regulations, UDI, EU authorized representative, UK responsible person.
Our client base covers start ups and micro companies with one or two employees right up to large multinationals. Our clients produce a wide range of medical devices from nanoparticles to hospital beds, from electronic monitors to coupling fluid & sterile products.
We offer a range of services so we can tailor the support we provide to meet our clients requirements. Our services are provided under our quality management system certified to ISO 13485:2016. For more information on the services we offer see our services page.