United States:
FDA Authorizes Emergency Use Of In Vitro Diagnostic Device For Enterovirus D68
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In the July 1, 2015, Federal Register, FDA announced
the issuance of an Emergency Use Authorization ("EUA")
for an in vitro diagnostic device to detect Enterovirus D68 strains
observed in North America in 2014. The EUA was issued pursuant to
the FDCA at the request of the Centers for Disease Control and
Preventions.
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