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NEW YORK (GenomeWeb) – The US Food and Drug Administration today announced it is easing the path for manufacturers who want to sell genetic health risk tests directly to consumers. 

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An announcement last week says laboratory-developed tests do not need to undergo premarket review by FDA.

As the Washington Post reports, President Donald Trump has made unfounded accusations against the FDA, saying it is part of the "deep state" and purposely causing delays.

The Associated Press reports India has boosted its COVID-19 testing ability, but may rely too much on antigen tests.

In PLOS this week: "dual-seq" transcriptomic analysis of bacterial cultures, genetic diversity among Hantaviridae, and more.

Oct
09
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As cases of COVID-19 continued to grow this spring and summer in the US, so too did the number of Emergency Use Authorizations from the FDA for clinical diagnostic tests aimed at detecting current and past infections.