FDA Issued Emergency Use Authorisation for COVID 19 Antigen Test
This is the second antigen test that the FDA has authorised for the detection of SARS-CoV-2 antigens
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US Food and Drug Administration
FDA takes additional step in harnessing real-world data to inform COVID-19 response efforts
Announcing participation in COVID-19 Diagnostics Evidence Accelerator, a multi stakeholder collaborative project to advance…
FDA clears Abbott’s next-generation FreeStyle Libre 2 iCGM system for adults, children ages four,…
Using Bluetooth technology, system automatically alerts users when their glucose is high or low without needing to scan the…
Gland Pharma launches RTU Bivalirudin Injection in US
This is the first non-frozen ready-to-use bivalirudin 505b(2) NDA approved by US FDA
FDA publicly shares antibody test performance data from kits as part of validation study
These results are among first to come from collaborative effort by FDA, NIH, CDC, BARDA
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FDA approves Roche immunotherapy cocktail in liver cancer
The immunotherapy Tecentriq in combination with drug Avastin will give speedy access to cancer patients
Swiss drugmaker Roche…
Cytokine Storm common in severe cases of COVID-19
Early studies suggest that up to 67 per cent of hospitalised COVID-19 patients may present with additional organ dysfunction…
FDA issues EUA for Abbott’s Alinity m molecular laboratory instrument
The automated platform can run more tests in less time to give laboratories improved efficiency, flexibility when using the…
Global researchers debate on the arrival of the COVID vaccine
Researchers contemplate the arrival by January or even further
Abbott launches third COVID-19 test
A lab-based serology blood test for detection of antibody, IgG, that identifies if a person has had COVID-19