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  <title><![CDATA[Semantically Rich Approach to Automating Regulations of Medical Devices]]></title>
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  <description><![CDATA[Advanced medical devices increasingly use sophisticated AI/ML models to enable real-time analytics for monitoring patients. In the US, these AI models, which often form the underlying device software, are regulated by the Center for Devices & Radiological Health (CDRH) at the Food & Drug Administration (FDA) to ensure the safety & efficacy of the medical device. These regulations for medical devices are currently available as large textual documents, called Code of Federal Regulations (CFR) T...]]></description>
  <dc:date>2024-07-11</dc:date>
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