Software as a medical device

Software as a medical device

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Software as a medical device
Software as a medical device
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As a SaMD manufacturer, you must ensure that your product meets the relevant regulatory requirements before being placed to the market.

It is critical to work with an EU Notified Body or UK Approved Body that understands the industry and has the experience to review and confirm your product’s readiness for market.


Thomas Doerge

Meet our experts

Our dedicated SaMD team brings extensive expertise in artificial intelligence, software development, and cybersecurity.