PerkinElmer Wins EUA to Test Asymptomatic PeoplePerkinElmer Wins EUA to Test Asymptomatic People

The company said based on comparative data released by FDA the test kit has the lowest Limit of Detection (LoD) among the authorized COVID-19 molecular diagnostic tests reported.

Omar Ford

January 14, 2021

2 Min Read
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PerkinElmer is targeting asymptomatic people in its latest testing offering for COVID-19 testing. The Waltham, MA-based company said it has received emergency use authorization from FDA for its Nucleic Acid Detection Kit to test individuals without symptoms or other reasons to suspect COVID-19 infection.

Here is the issue. About 60% of total COVID-19 transmissions come from those who have no symptoms, signaling that silent spreaders are the ones most often passing the virus around without knowing it, according to a new model from The Journal of the American Medical Association’s Open Network developed by researchers from the Centers for Disease Control and Prevention.

The Waltham, MA-based company said based on comparative data released by FDA the test kit has the lowest Limit of Detection (LoD) among the authorized COVID-19 molecular diagnostic tests reported, deeming it the most sensitive assay.

“The data is clear – it’s imperative we have reliable and accurate testing for asymptomatic individuals, especially as we’re seeing new strains of the virus appear that are even more contagious,” Masoud Toloue, PhD, Vice President & General Manager, Diagnostics, PerkinElmer, said in a release. “PerkinElmer is in a unique position to help this cause, as we’re one of the few suppliers to have an EUA for asymptomatic testing, maintain the most sensitive test on the market along with a strong supply chain, and have the capability to do sample pooling to save time and resources for diagnostic laboratories.”

LabCorp was one of the first companies MD+DI reported about receiving an indication for asymptomatic testing. In July of 2020, FDA said it reissued the LabCorp COVID-19 RT-PCR Test EUA to expand the use of the test to anyone after the company provided scientific data showing the test’s ability to detect SARS-CoV-2 in a general, asymptomatic population.

The Burlington, NC-based has had EUA for its SARS-CoV-2 tests since the onset of the pandemic in the U.S.

 

About the Author

Omar Ford

Omar Ford is a veteran reporter in the field of medical technology and healthcare journalism. As Editor-in-Chief of MD+DI (Medical Device and Diagnostics Industry), a leading publication in the industry, Ford has established himself as an authoritative voice and a trusted source of information.

Ford, who has a bachelor's degree in print journalism from the University of South Carolina, has dedicated his career to reporting on the latest advancements and trends in the medical device and diagnostic sector.

During his tenure at MD+DI, Ford has covered a wide range of topics, including emerging medical technologies, regulatory developments, market trends, and the rise of artificial intelligence. He has interviewed influential leaders and key opinion leaders in the field, providing readers with valuable perspectives and expert analysis.

 

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