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https://forsante.com/wp-content/uploads/2024/01/Forsante-1.png10001109Forsante Ltd has been granted an EU Medical Devices MDR certification by SGS. Obtaining the certification requires the medical device to meet strict patient safety and system requirements. The IRMA AI module from Forsante is now CE-marked in the demanding Class 2b risk category and, to our knowledge, is the first clinical decision support solution […]