Software, hardware and digital product development: experts meet here!
Software manufacturers and service providers in medical technology are faced with the high demands of a strictly regulated industry. That is because their solutions are very often integral parts of products and devices that are subject to the Medical Device Directive (MDR) and the ISO 13485 and IEC 62304 standards. Equally demanding is the development of solutions that do not necessarily have to meet strict regulations themselves but must blend in perfectly with existing processes. They are used in production management and areas such as ERP, CRM and CAD, and are indispensable in manufacturing and production and in placing the products on the market.