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Kyverna Therapeutics Granted FDA Fast Track Designation for KYV-101 in the Treatment of Pa

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Coperion optimises extruder design for greater flexibility

Coperion has equipped its ZSK 18 MEGAlab laboratory extruder with numerous new functions that are designed to provide gr

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Regulatory Update — Week of Jan. 15, 2024

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Bidirectional Link ID'd for Autoimmune Disease, Perinatal Depression

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COVID-19 Vaccine Uptake More Likely in Pregnancy if Receiving Other Vaccines

FRIDAY, Jan. 19, 2024 -- Pregnant patients are more likely to accept COVID-19 vaccination if they receive other routine

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Possible Link Found Between Video Gaming, Hearing Loss/Tinnitus

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Clinical Practice Guideline Developed for Management of Pouchitis

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Nuance AI copilot now fully embedded in Epic EHR

More than 150 hospitals and health systems currently use the DAX Copilot in their Epic electronic health record workflow

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MESQUITE, NV, Jan. 19, 2024 (GLOBE NEWSWIRE) -- via NewMediaWire – United Health Products (UEEC) reports today on the receipt and review of final reports on product sterilization and stability testing for its hemostatic gauze. As previously disclosed, UHP has been working with external packaging and sterilization service providers to complete various required tests for its Premarket Approval application. The reported data received this week on the efficacy of the proposed radiation sterilization protocol were well within acceptable bioburden levels for Class III products. UHP will now compile these data and proceed with final drafting of the PMA documentation to be submitted via the eSTAR platform for FDA and Health Canada review.

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MESQUITE, NV, Jan. 19, 2024 (GLOBE NEWSWIRE) -- via NewMediaWire – United Health Products (UEEC) reports today on the receipt and review of final reports on product sterilization and stability testing for its hemostatic gauze. As previously disclosed, UHP has been working with external packaging and sterilization service providers to complete various required tests for its Premarket Approval application. The reported data received this week on the efficacy of the proposed radiation sterilization protocol were well within acceptable bioburden levels for Class III products. UHP will now compile these data and proceed with final drafting of the PMA documentation to be submitted via the eSTAR platform for FDA and Health Canada review.

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