Thursday, April 1, 2021

FDA Authorizes Over-the-Counter and Other Screening Tests for COVID-19

The addition of the OTC indications gives schools, workplaces, and others several options for serial screening tests

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US Food and Drug Administration

COVID-19 Update: FDA Continues to Advance Over-the Counter and Other Screening Test Development

On March 31, the U.S. Food and Drug Administration (FDA) authorized several COVID-19 tests for over-the-counter (OTC) use without a prescription when used for serial screening (testing asymptomatic individuals multiple times on a routine basis), such as testing twice a week in schools or other settings. The FDA also authorized serial screening tests for use in a point-of-care (POC) setting, such as a doctor's office. These authorizations follow the FDA's recent actions to advance OTC and other screening test development. These tests:

  • Can be used to test people with or without COVID-19 symptoms.
  • Are antigen tests that detect proteins from SARS-CoV-2, the virus that causes COVID-19, from a nasal swab sample.
  • Give results in 10-30 minutes without needing to send a sample to a laboratory for analysis.

Specific tests authorized yesterday:

  • Quidel QuickVue At-Home OTC COVID-19 test - authorized for OTC at-home serial screening
  • Abbott BinaxNOW (multiple configurations)
    • Abbott BinaxNOW COVID-19 Antigen Self Test - authorized for OTC at-home serial screening
    • Abbott BinaxNOW COVID-19 Ag Card 2 Home Test - authorized for OTC at-home serial screening with telehealth proctor
    • Abbott BinaxNOW COVID-19 Ag 2 Card - authorized for POC serial screening without a prescription
  • BD Veritor System for Rapid Detection of SARS-CoV-2 - authorized for POC serial screening with a prescription

Read More

Questions?

If you have questions, email COVID19DX@fda.hhs.gov.


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