USE-ME-D SRL deals with providing consultancy support at the level of management of the Quality, Regulatory and Usability system of medical devices.
Usability consulting services, from device design to marketing. Specialized in usability studies for both formative and summative evaluations of the device user interface and in the creation of reporting in compliance with IEC 62366. It provides regulatory consultancy services throughout the life cycle of the medical device. It is aimed at medical device manufacturers who wish to develop an innovative medical device and obtain CE certification, in accordance with the MDR 2017/745 Regulation. Specialized in software assistance, design and validation, including AI.