Search For "food and drug administration"
Study: Colleges can prevent 96 pc of COVID-19 infections with common measu
Updated : 5 years, 2 months ago IST
Washington [US], January 13 (ANI): The combined effectiveness of three COVID-prevention strategies on college campuses--mask-wearing, social distancing, and routine testing--are as effective in preventing coronavirus infections as the Pfizer and Moderna vaccines approved by the U.S. Food and
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LASA receives WHO Nod for its Khed Unit in Ratnagiri
Updated : 5 years, 2 months ago IST
Mumbai (Maharashtra) [India], January 12 (ANI/NewsVoir): API major, Lasa Supergenerics Ltd. Received WHO Certificate of Good Manufacturing Practices from the Food and Drug Administration authorities for its manufacturing facility situated at Khed (Ratnagiri).
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US FDA probing 'about five' allergic reactions to Pfizer COVID-19 vaccine
Updated : 5 years, 3 months ago IST
Washington [US], December 19 (ANI/Sputnik): The US Food and Drug Administration (FDA) is probing roughly five instances of individuals having allergic reactions to Pfizer and BioNTech's vaccine against COVID-19, Peter Marks, the director of the FDA's Center for Biologics Evaluation and Resea
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US FDA authorises Moderna Covid-19 vaccine for emergency use
Updated : 5 years, 3 months ago IST
Washington [US], December 19 (ANI): The United States Food and Drug Administration's (FDA) on Friday (local time) has authorised Moderna coronavirus vaccine for emergency use for people aged 18 years and above.
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US FDA plans to give Moderna authorisation for emergency use
Updated : 5 years, 3 months ago IST
Washington [US], December 18 (ANI): Advisors to the US Food and Drug Administration (FDA) voted in favour to recommend that the agency must give Emergency Use Authorisation (EUA) to Moderna's COVID-19 vaccine.
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Trump, White House staffers not among first to get COVID vaccine
Updated : 5 years, 3 months ago IST
Washington [US], December 14 (ANI): Days after the US Food and Drug Administration approved the Pfizer COVID-19 vaccine for emergency use, President Donald Trump on Sunday (local time) said that he along with the White House (WH) staffers would not be among the first in the country to get th
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UPS, FedEx collaborate to ship Pfizer-BioNTech Covid-19 vaccines in US
Updated : 5 years, 3 months ago IST
Washington [US], December 13 (ANI): Rival US companies UPS and FedEx are working side-by-side to ship the Pfizer-BioNTech Covid-19 vaccine, after it was approved for emergency use by the US Food and Drug Administration (FDA) on Friday.
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Pfizer Covid Vaccine will be administered in less than 24 hours, says Trum
Updated : 5 years, 3 months ago IST
Washington [US], December 12 (ANI): Soon after the US Food and Drug Administration on Friday approved Pfizer's COVID-19 vaccine for emergency use across the country, President Donald Trump said that the vaccine will be administered "in less than 24 hours."
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US FDA authorizes Pfizer's COVID-19 vaccine for emergency use
Updated : 5 years, 3 months ago IST
New York [US], December 12 (ANI): The US Food and Drug Administration authorized Pfizer's Covid-19 vaccine for emergency use on Friday for the prevention of coronavirus disease in individuals 16 years of age and older.
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FDA panel nod to emergency use approval for Pfizer vaccine
Updated : 5 years, 3 months ago IST
Washington [US], December 11 (ANI): A panel of experts advising the US Food and Drug Administration (FDA) on Thursday recommended emergency approval for the Pfizer-BioNTech Covid-19 vaccine.
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COVID-19: Moderna submits vaccine data to obtain emergency use authorisati
Updated : 5 years, 3 months ago IST
Washington DC [US], December 1 (ANI): US biotech company Moderna said that it has submitted the results of its coronavirus vaccine trials to the country's Food and Drug Administration (FDA) in order to obtain emergency use authorisation for the vaccine.
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Moderna to request Emergency use authorisation, its vaccine 100% effective
Updated : 5 years, 3 months ago IST
Washington [US], November 30 (ANI): US biotech company Moderna on Monday announced that it plans to request an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) and conditional approval from the European Medicines Agency (EMA) after the final results from a lat
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