Certified for the future

XITASO is constantly evolving, and that also applies to the highly demanding medical engineering branch. Especially here, certifications are an important way of emphasizing that we can provide our customers with excellent support. Often, they are even a precondition for the implementation of our customer’s projects.

XITASO proudly presents: ISO 13485

We are delighted that the MedTech sector from XITASO has been certified according to ISO 13485. In accordance with this standard, we can develop software independently for our customer’s medical products and thus give them the crucial advantages. With the ISO 13485 certification, we can now deliver self-contained components without the complicated process of integrating our work into our customers' quality management systems. We therefore take on full responsibility. This means we can now work even better with our customers, take on additional tasks and let them benefit from the quality of our work and our expertise.

In focus: patient security

In the medical engineering industry in particular, (software) products must function safely. ISO 13485 therefore places particular emphasis on patient security. To ensure this, for instance, it is crucial to carefully assign and document all processes with clear responsibilities in order to enable comprehensive tracking. In this context, measures to ensure cyber security are also firmly integrated into the development process pursuant to IEC 62304. We dedicate ourselves to precisely analysing potential threats and implementing targeted measures for avoiding these risks.

An important step towards the future

Medical technology is an important market for XITASO. Many customers have been relying on our specific expertise in medical technology for years now and collaborate with us from prototype development through to the certified medical device. With our high level of expertise, we contribute to excellent digital solutions and thus do socially relevant work.

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