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Clinical phenotype, in silico and biomedical analyses, and intervention for an east Asian population-specific c

( We agree with the applicant that the Nelli Seizure Monitoring System meets the cost criterion and are therefore proposing to approve the Nelli Seizure Monitoring System for new technology add-on payments for FY 2024, subject to the technology receiving FDA marketing authorization as a Breakthrough Device for the indication corresponding to the Breakthrough Device designation by July 1, 2023

And I think that it would be very interesting, sort of, path to go down but, again, there's so many things I don't know at the moment, I'm just trying to focus on the ones that I do know

The process ensures purity and precise dosing, as administration is intravenous only and should be performed by trained healthcare personnel