Etiometry, a leader in clinical decision-support software for critical care, announced that the company has obtained the CE Mark under the European Union’s medical device regulation, marking the second adult and third pediatric market authorization. Etiometry’s AI-powered clinical decision tool helps clinicians identify subtle signs of deterioration and enable effective care coordination, with published evidence demonstrating decreased length of stay and readmissions.
The certification will allow for the use of the Etiometry platform and algorithms that use models of human physiology to interpret patient data into individualized risk assessments in the European Union (EU) and the United Kingdom (UK). This is the latest regulatory milestone for Etiometry, which has received seven FDA clearances and two Health Canada approvals and opens the door to expansion in Europe for the rapidly growing company.
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