The World Health Organization (WHO) has listed the first mpox in vitro diagnostic (IVD) under its Emergency Use Listing (EUL) procedure, an important step in improving global access to mpox testing.
The World Health OrganizationOct 4 2024 The World Health Organization has listed the first mpox in vitro diagnostic under its Emergency Use Listing procedure, an important step in improving global access to mpox testing. The approval for emergency use of the Alinity m MPXV assay, manufactured by Abbott Molecular Inc., will be pivotal in expanding diagnostic capacity in countries facing mpox outbreaks, where the need for quick and accurate testing has risen sharply.
The presence of the monkeypox virus is confirmed by nucleic acid amplification testing , such as real-time or conventional polymerase chain reaction , as stated in the WHO Interim Guidance on Diagnostic testing for the monkeypox virus . And the recommended specimen type for diagnostic confirmation of monkeypox virus infection in suspected cases is lesion material.
This first mpox diagnostic test listed under the Emergency Use Listing procedure represents a significant milestone in expanding testing availability in affected countries. Increasing access to quality-assured medical products is central to our efforts in assisting countries to contain the spread of the virus and protect their people, especially in underserved regions.
Mpox Assay DNA In Vitro IVD Laboratory Virus
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