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In the September 1, 2015, Federal Register, FDA announced the issuance of an EUA for an in vitro diagnostic device for detection of Middle East Respiratory Syndrome Coronavirus (MERS-CoV).
United StatesFood, Drugs, Healthcare, Life Sciences
In the September 1, 2015, Federal Register,
FDA announced the issuance of an EUA for an in vitro diagnostic
device for detection of Middle East Respiratory Syndrome
Coronavirus (MERS-CoV). FDA issued this authorization under the
FDCA, as requested by altona Diagnostics GmbH.
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