Publications

24.06.2026

ISO 13485: Key features of the standard for medical device manufacturers

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08.06.2026

Stand-alone software as a medical device: classification and conformity assessment

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01.06.2026

Training of medical device manufacturers' personnel as part of the quality system

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25.05.2026

Certification of medical devices as a guarantee of patient safety

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18.05.2026

Risk management in the production of medical devices: tools for assessing and minimizing risks to patient safety

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11.05.2026

The soldering process of electronic components of medical equipment. Why is it necessary to validate it?

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