LNE, GMED’s parent company, and INRIA have just signed a framework agreement defining their roadmap, with the aim of setting up an “AI Evaluation” program. This strategic partnership will take the form of an evaluation center carrying out research, experimentation and control activities at the highest world level in AI. LNE will act as the French national reference laboratory for AI evaluation.
GMED, as a notified body for medical devices and in vitro diagnostic medical devices, certifies devices incorporating AI. We keep developing our skills along with LNE to meet the future AI stakes in the various international regulatory frameworks, and so offer all the industrial players concerned an AI assessment and certification service, in line with the state of the art in regulations.
To certify your AI-enabled devices or for more information: https://lne-gmed.com/contact-offices
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