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GetMyDNA Receives EUA for COVID-19 Test Home Collection Kit for DTC Purchase
americanpharmaceuticalreview
March 19, 2021
The U.S. Food and Drug Administration (FDA) issued emergency use authorization (EUA) to launch the GetMyDNA COVID-19 Test Home Collection Kit DTC, which is now available for broad use for both symptomatic and asymptomatic individuals with no ...
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Novartis in discussions to help produce COVID-19 vaccines, tests
expresspharma
January 29, 2021
Novartis last year agreed to license two of Molecular Partners’ antiviral drugs that it hopes to use to treat COVID-19 patients.
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eMed™ Announces Partnership with the State of Ohio to Provide Millions of BinaxNOW™ At-Home COVID-19 Rapid Tests
prnewswire
January 22, 2021
eMed™ announced a partnership with the State of Ohio to distribute and administer at least 2 million virtually-guided, BinaxNOW™ at-home COVID-19 rapid tests, which deliver results within minutes.
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FDA GRANTS ADVAITE EMERGENCY USE AUTHORIZATION FOR RapCov™ Rapid COVID-19 Test
prnewswire
January 13, 2021
The U.S. Food and Drug Administration has granted Emergency Use Authorization (EUA) to one of the first U.S.-manufactured serology tests designed by ADVAITE Inc., an innovative biotech company developing novel point-of-care assays to help with ...
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Beckman Coulter Launches High-Throughput COVID-19 Antigen Test
americanpharmaceuticalreview
December 28, 2020
Beckman Coulter announced the launch of a new test that addresses the three main barriers currently facing schools, businesses, hospitals and communities with the rollout of mass COVID-19 testing.
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FDA Authorizes COVID-19, Flu Combination Test with Home-Collected Samples
americanpharmaceuticalreview
December 24, 2020
The U.S. Food and Drug Administration (FDA) authorized the first diagnostic test for at home collection of patient samples to detect both COVID-19 and influenza A and B (flu).
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Aptar CSP Increases Capacity for Active Packaging Solutions
contractpharma
December 18, 2020
3-Phase Activ-Polymer platform technology protects electrochemical, lateral flow, and molecular diagnostic test kits.
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FDA Authorizes BinaxNOW COVID-19 Ag Card Home Test
americanpharmaceuticalreview
December 18, 2020
The U.S. Food and Drug Administration (FDA) issued a new emergency use authorization (EUA) for the BinaxNOW COVID-19 Ag Card Home Test which is authorized for use by patients at home with a prescription.
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Cipla launches rapid antigen detection test to diagnose COVID-19
expresspharma
December 16, 2020
Cipla announced its partnership with the Premier Medical Corporation for commercialisation of the rapid antigen test kits for COVID-19 in India. The company will commence supply from this week.
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CDSCO to identify and set up two additional facilities for testing COVID-19 vaccines
expresspharma
December 14, 2020
The CDSCO has identified the challenges associated with COVID-19 vaccines are taking steps to mitigate them, informs Dr Eswara Reddy.