The U.S. General Services Administration (GSA) is entering into a partnership with the U.S. Food and Drug Administration (FDA) as part of GSA’s Centers of Excellence (CoE) initiative, housed within GSA's Technology
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NASA engineers have developed a new high-pressure ventilator to treat COVID-19 patients and it has been approved by the Food and Drug Administration (FDA) for under the ventilator Emergency Use Authorization (EUA),
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The FDA has announced that the administration will expand access to serology tests and its approach to making accurate and reliable serology tests widely available, while also protecting Americans from tests marketed
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The Department of Veterans Affairs, Food and Drug Administration and National Institutes of Health are working with nonprofit organization America Makes to accelerate the manufacture of personal protective equipment, Federal News Network reported
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Regeneron Pharmaceuticals has announced that the U.S. Food and Drug Administration (FDA) has accepted for Priority Review a new Biologics License Application (BLA) for REGN-EB3, an investigational triple antibody treatment for Ebola
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The U.S. Food and Drug Administration issued an emergency use authorization (EUA) that has the potential to decontaminate approximately 4 million N95 or N95-equivalent respirators per day in the U.S. for reuse
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The U.S. Food and Drug Administration (FDA) has developed a new program across public, academic and private sectors to combat the COVID-19 pandemic, the administration reported on Tuesday.
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The Department of Veterans Affairs, Food and Drug Administration and National Institutes of Health have launched a joint research and development initiative focused on using additive manufacturing to address medical equipment shortages,
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Battelle has received Food and Drug Administration (FDA) Emergency Use Authorization (EUA) to support front-line healthcare workers as they face critical shortages of personal protective equipment (PPE), the company announced on Sunday.
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PerkinElmer has announced today that the U.S. Food and Drug Administration (FDA) has provided Emergency Use Authorization (EUA) for the Company’s New Coronavirus RT-PCR test.
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