FDA issues emergency authorisation for remdesivir to treat COVID-19
The U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for emergency use of Gilead’s remdesivir
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Regulatory
Shionogi receives EC approval for new antibiotic FETCROJA® (cefiderocol)
Japanese research-driven pharmaceutical company Shionogi & Co., Ltd. and its European subsidiary, Shionogi B.V. announced on April 28 that the
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Sanofi’s MenQuadfi meningococcal (MenACWY) vaccine gets FDA nod
The FDA has shown green light for MenQuadfi, Sanofi’s innovative meningococcal (MenACWY) vaccine. The U.S. Food and Drug Administration (FDA)
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FUJIFILM’s Avigan Tablet for COVID-19 to be Free for 20 Countries
While COVID-19 transmission is expanding, the Japanese government has agreed to raise its Avigan® Tablet (favipiravir) stockpile, which is estimated
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The top 10 Pharmaceutical Innovation Index companies 2020
Success on the Innovation Index is important, especially now, at a time when innovation is needed more than ever. Many,
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Abbott’s molecular point-of-care COVID-19 test could be a gamechanger
At the end of March, the American medical devices and healthcare company Abbott Laboratories announced that the U.S. Food and
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FDA grants Emergency Use Authorisation for Roche’s Coronavirus Test
Roche’s coronavirus test has been granted Emergency Use Authorization by the U.S. Food and Drug Administration, the Swiss pharma giant
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