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Aug 29 (Reuters) - The World Health Organization on Thursday sought to speed up the access to diagnostic tests for mpox by asking manufacturers to submit their products for an emergency review.
The agency has been in discussions with manufacturers about the for effective diagnostics, particularly in low-income groups.
To expand access to diagnostic services urgently, the WHO has called for submissions from manufacturers for Emergency Use Listing that would allow it to approve medical products such as vaccines, tests and treatments.
The process aims to assist countries to procure the critically products such as tests through UN agencies and other partners.
A form of the virus has triggered global concern as it seems to spread easily though routine close contact, prompting the health agency to declare mpox a global public health emergency earlier this month.
Sweden and Thailand have confirmed cases of the clade Ib type of the virus, outside of the Democratic Republic of Congo and countries.
With as many as 1,000 suspected cases reported in the Congo alone this week, the for diagnostic tests has surged dramatically, the agency said.
In the coming weeks, it will deliver another 30,000 tests to African countries.
The WHO has also updated its diagnostic testing guidance to detect the virus strain and is working with counties to roll it out.
Manufacturers of in-vitro diagnostics have been asked to provide available data on the quality, safety and performance of the tests to the WHO as soon as possible.
Earlier this week, diagnostics firm Labcorp LH.N said it is working with U.S. health regulators to determine if it to ramp up its mpox testing capacity.
Swiss drugmaker Roche ROG.S is actively working to enhance laboratory testing capacity for mpox worldwide.
(Reporting by Sriparna Roy in Bengaluru; Editing by Mohammed Safi Shamsi and Arun Koyyur)