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On September 28, 2022, the Food and Drug Administration (FDA) issued Clinical Decision Support Software final guidance. The guidance clarifies the agency’s scope of oversight and regulation of clinical decision support software based on the definition of a device in the Federal Food, Drug, and Cosmetic Act (FD&C Act). It also describes the criteria used to assess whether software functions do not meet the definition of a device.
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Clinical-grade wearables include regulated devices and supporting platforms that are generally certified/approved for use by one or more regulatory or health authorities, such as the U.S. Food and …
Posted Oct 11, 2022 Healthcare Internet of Medical Things (IOMT)
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