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Tag Archives: HMI

Usability one key to success

by Marcus Zingmark, February 18, 2013, 
(209)

For about 6 years ago Apple changed a whole world on the expectations we have on cellulars and its user interfaces. Before the first iPhone was released a cellular had physical buttons and the focus was to have great technology in a small shell with great battery capacity. Now the world has completely changed.

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Customer’s demand causing headache for the automotive industry

by Kaarle Honkamaa, September 27, 2012, 
(439)

Today pleasing car buyers is not an easy task, not only because of current economic climate. When consumers plan to purchase a new car they will look at the same features as before like appearance, safety, performance and increasingly also fuel economy. Now, buyers put more and more emphasis also on the infotainment (IVI) capabilities of the car when making their buying decisions. In fact, according to recent studies, almost 50% of buying decisions are [...]

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Do we need to have more Linux in our cars?

by Peter Seidenschwang, September 21, 2012, 
(1365)

Your PC/Laptop runs with Windows? Your mobile phone and tablet runs with Android? How do you feel about your car running with Linux? Most probably you are not interested in what technical basis the infotainment system in your car is built on?

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The semiconductor manufacturer as a mediator for In-Vehicle-Infotainment Solutions

by Günter Zettler, August 19, 2012, 
(173)

In-Vehicle-Infotainment (IVI) has changed with fast speed within the last 20 years. There is an obvious trend of consuming multimedia and entertainment services in the car which we are already used to at home; typical smart products connected to the internet with high usability and excellent user experience …

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ISO 13485 Surveillance Audit successfully conducted

by Siegfried Hörfarter, May 28, 2012, 
(140)

With our Embedded Systems business we have successfully conducted the ISO 13485 surveillance audit. We are already holding the ISO 13485 certification since April 2010. The ISO Standard defines the regulatory quality management requirements for design and production of medical devices and products. The surveillance audit must be performed on a regular base every year; and our next Re-Certification is planned in 2013.

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