More COVID-19 Testing Relief Is on the Way

HHS is further investing in rapid COVID-19 testing. Here’s how.

Omar Ford

November 11, 2021

1 Min Read
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Alamy/Shreenath s puranik

COVID-19 testing is getting another infusion of funding. The Department of Health and Human Services said it will invest $650 million from the American Rescue plan to strengthen manufacturing capacity for quick, high-quality diagnostic testing through rapid point-of-care molecular tests and increase access.

As at-home testing increases, the need for follow-up testing in health care settings will likely grow. For example, if someone buys an over-the-counter rapid antigen test at their local pharmacy to take at home and tests positive, they may seek out a health care provider who would conduct another test to confirm that result. This new investment will help ensure tests like these are readily available across the country and can provide results quickly.

“Access to fast, accurate, and reliable tests help keep Americans safe and healthy,” HHS Secretary Xavier Becerra, said in a release. “Thanks to the American Rescue Plan, we are increasing our testing supply, investing in American manufacturers, and continuing to support these critical tools for getting the pandemic under control.”

The funding follows $1 billion ear-marked by the Biden Administration, in October, to keep up with the increased demand for the diagnostics.

Last month’s initiative follows a September measure from the administration authorizing $2 billion to ensure tests are available to those who need them and to provide manufacturers with purchase commitments that allow them to ramp up their production.

 

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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