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14 held, Rs 35 lakhs seized in Karnataka PSC exam leak
Updated : 5 years, 1 month ago IST
Bengaluru (Karnataka) [India], January 24 (ANI): The total number of people who have been arrested in the Karnataka Public Service Commission First Division Assistant (FDA) examination paper leak case has reached 14 on Sunday, the police informed.
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Karnataka PSC FDA exam postponed after question paper leak
Updated : 5 years, 1 month ago IST
Bengaluru (Karnataka) [India], January 23 (ANI): Karnataka Public Service Commission (KPSE) on Saturday postponed the First Division Assistant (FDA) examination, which was scheduled to be held on January 24 after six people were arrested and question paper was seized from their possession.
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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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Glenmark receives one ANDA approval and two tentative ANDA approvals - Tad
Updated : 5 years, 2 months ago IST
Mumbai (Maharashtra)[India], December 31 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark), a research-led global pharmaceutical company has received final approval by the United States Food & Drug Administration (U.S. FDA) for Tadalafil Tablets USP, 2.5 mg, 5 mg, 10 mg and 2
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Fluidigm's FDA-EUA Authorized Saliva-based SARS-CoV-2 RT-PCR Assay - Now f
Updated : 5 years, 2 months ago IST
New Delhi [India], December 24 (ANI/NewsVoir): It's been a year now since the first few human cases of COVID-19 infection were reported amidst the busy wholesale food market of China's Wuhan city. The disease caused by SARS-CoV-2 virus, thought to have its origin in Bats, soon spread to caus
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Glenmark Pharmaceuticals receives ANDA tentative approval for Dabigatran E
Updated : 5 years, 3 months ago IST
Mumbai (Maharashtra) [India], December 21 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received tentative approval by the United States Food & Drug Administration (U.S. FDA) for Dabigatran Etexilate Capsules, 75 mg, 110 mg, and 150 mg, the generic version of Pradaxa®
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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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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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