European Medical Device Regulation

Stephanie Ward, a quality assurance engineer at technology and product design firm Cambridge Design Partnership looks at the new European medical devices regulation in more detail and the impact these may have on manufacturers. more


Proactivity and due diligence are the key to success for new MDR roll-out, says Peter Rose, Maetrics more


Maetrics reveals the practical implications for medical device manufacturers and how to address them as the new MDR comes into force. more