HANNOVER MESSE 2019, 01 - 05 April
macio
Safety plays a significant role in medical technology. For hardly any other sector the reliability and safety of devices and machines is as essential as it is for the medical sector. Requirements concerning software for medical technology are particularly high as are result. macios quality management system for the sector of medical devices is DIN EN ISO 13485:2012 certified. Furthermore, reliability and safety is achieved through IEC 62304-compliant development. Upon request we edit the software product development including a comprehensive support on the risk management for the licensing. QMS and norms DIN EN ISO 13485 | QMS - Requirements for regulatory purposes DIN EN 62304 | Medical device software - Software lifecycle processes EN 62366 | Application of usability engineering to medical devices DIN EN ISO 14971 | Application of risk management to medical devices
VDMA Pavilion - Software
The requirements towards modern software solutions are getting higher and higher. Only the combination of different software technologies, future-oriented technological ... more
Our user interfaces combine well-structured operational concepts, intuitive controls, latest input methods and modern, appealing designs. Operating safety is our ... more
Die macio GmbH unterstützt Sie bei der Analyse Ihres Vorhabens - von der Ideenphase bis hin zur Umsetzung in ein marktfähiges Produkt. Auf diesem Weg stehen wir ... more
Sie wollen Fehlfunktionen einer Maschine direkt aus der Ferne beheben? Mobile Apps sollen die Maschinenbedienung erleichtern? Immer mehr Alltagsgegenstände und technische ... more
High-efficiency pumps, medical scales and wind turbines have one thing in common: All these technologies work with embedded systems, that are cost-effective and ... more
Apps for mobile devices, like smartphones and tablets, did not capture the consumer market only, but also the shop floors. Apps allow to gain location-independent ... more
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