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9 Technologies That Will Shape The Future Of Dentistry

The Medical Futurist

For dentists, it’s transforming diagnosis, decision-making, and treatment planning. In comparison, the first VR-recorded surgery was performed at the Royal London Hospital in 2016. Its importance was also highlighted during the COVID-19 crisis to bypass supply chains to meet hospitals’ demands.

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The Healthcare Vision of ChatGPT-4o and Multimodal LLMs

The Medical Futurist

Finally, the arrival of interoperability can connect and harmonise various hospital systems An M-LLM could serve as a central hub that facilitates access to various unimodal AIs used in the hospital, such as radiology software, insurance handling software, Electronic Medical Records (EMR), etc. AI used in the hospital.

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The Future Of Vision And Eye Care

The Medical Futurist

In 2016, The Guardian reported that a blind woman suffering from this disease was fitted with the implant labelled “bionic eye” in the UK as part of a trial at the Oxford Eye Hospital. A year later, the search giant announced they have begun working on integrating the technology into a chain of eye hospitals in India.

Diabetes 105
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Out At Home: FDA’s Vocal Support of Home Testing but Reluctance to Clear Novel OTC Home Tests

FDA Law

He also identified “Next-Generation Home-based Testing Technologies, including new IVDs, Digital Lateral Flow Readers, and Reporting Technologies” as an opportunity to “extend care from the hospital and clinic into the home setting.” HbA1c, diagnosis of a particular virus, etc.). dried blood, in viral transport media).

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CMS Final Medicaid Drug Rebate Rule Details New Misclassification Penalties and Numerous Other Changes

FDA Law

CMS did not finalize the price verification survey, which would have required manufacturers of 10 costly drugs selected annually to provide clinical information as well as information on production, distribution, research, and marketing costs, revenue and profit, and ex-U.S. Remarkably, manufacturers may not dispute a CMS notification.

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New Breakthrough Devices Program Guidance: Expanding Opportunities for Medical Product Innovations

FDA Law

This implies that if device technologies and features can produce a clinically meaningful impact for the treatment or diagnosis of a condition in certain populations, such data could support the case that the device satisfies the first designation criterion. Other Updates With respect to the first part of the first criterion (i.e.,

Medical 53
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Joint Basis for FDA/HHS Marijuana Rescheduling Recommendation Unveiled

FDA Law

whether growing or not; its seeds; resin extracted from any part; and every compound, manufacture, salt, derivative, mixture, or preparation of the plant, its seeds or resin. “Marijuana,” subject to the rescheduling recommendation, means all parts of the plant Cannabis sativa L., 21 U.S.C. § 802(16)(A). 21 U.S.C. § 802(16)(B).

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