Search For "us food and drug administration"
FDA denies authorization to market JUUL e-cigarettes over safety concerns
Updated : 3 years, 9 months ago IST
Maryland [US], June 24 (ANI): Citing safety concerns, the US Food and Drug Administration (FDA) issued marketing denial orders (MDOs) to JUUL Labs Inc. for their e-cigarettes among others which are currently marketed in the United States.
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Blood test that can detect breast cancer, available in India now
Updated : 3 years, 9 months ago IST
New Delhi [India], June 22 (ANI): In a first-of-its-kind, a blood test can detect breast cancer at very early stages. It has been launched in India on Wednesday and has been made available by Datar Cancer Genetics, a private company which has partnered with the Apollo group of hospitals.
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US approves Pfizer, Moderna Covid-19 vaccines for youngest children
Updated : 3 years, 9 months ago IST
Washington [US], June 17 (ANI): The US Food and Drug Administration (FDA) authorized emergency use of the Moderna COVID-19 Vaccine and the Pfizer-BioNTech COVID-19 Vaccine for the prevention of COVID-19 to include use in children down to 6 months of age.
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FDA removes hold on clinical trial for phase 2,3 for COVAXIN-BBV152 says
Updated : 3 years, 10 months ago IST
Malvern (Pennsylvania) [US], May 23 (ANI): Biotechnology company Ocugen on Monday announced that the US Food and Drug Administration (FDA) lifted the clinical hold on the Company's Phase 2, 3 clinical trials for COVAXIN™ (BBV152).
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US FDA limits use of Johnson & Johnson COVID-19 vaccine over blood clo
Updated : 3 years, 10 months ago IST
Washington [US], May 6 (ANI): The US Food and Drug Administration (FDA) on Thursday said that the Johnson & Johnson vaccine that has been administered to more than 18 million Americans can potentially cause "life-threatening blood clots", and thereby warranted "limiting the authorized us
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COVID-19: FDA gives clearance to Covaxin for clinical trials in adults in
Updated : 4 years ago IST
New Delhi [India], March 7 (ANI): Bharat Biotech's COVID-19 vaccine Covaxin has been given clearance for clinical trials in adults by the US Food and Drug Administration (FDA).
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US FDA grants the coveted Breakthrough Designation for early-stage prostat
Updated : 4 years, 1 month ago IST
Mumbai (Maharashtra) [India], February 15 (ANI/PR Newswire): Datar Cancer Genetics today announced that the US Food and Drug Administration (FDA) has granted 'Breakthrough Designation' for its blood test to detect early-stage prostate cancer. This is the second test from the Company that has
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Rapid antigen tests less sensitive for detecting Omicron variant infection
Updated : 4 years, 2 months ago IST
Washington [US], December 29 (ANI): The Food and Drug Administration in the US has said that rapid antigen tests are less sensitive for detecting Omicron variant infections.
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US grants emergency use authorization for Merck's COVID-19 pill
Updated : 4 years, 2 months ago IST
Washington [US], December 23 (ANI): The US Food and Drug Administration (FDA) on Thursday said that it has granted an emergency use authorization for Merck's antiviral pill Molnupiravir that is used to treat COVID-19 patients.
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US FDA authorizes Pfizer's COVID antiviral pill for people aged 12
Updated : 4 years, 2 months ago IST
.Washington [US], December 23 (ANI): The US Food and Drug Administration (FDA) on Wednesday (local time) authorized Pfizer's Paxlovid COVID-19 pill for high-risk people aged 12 and over to treat coronavirus disease (COVID-19).
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US FDA grants breakthrough designation for early-stage breast cancer detec
Updated : 4 years, 4 months ago IST
Mumbai (Maharashtra) [India], November 20 (ANI/PRNewswire): Datar Cancer Genetics, a leading cancer research company today announced that the US Food and Drug Administration (FDA) has granted 'Breakthrough Designation' for its blood test to detect early-stage Breast Cancer.
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COVID-19: US FDA expands emergency use authorizations for Pfizer, Moderna
Updated : 4 years, 4 months ago IST
Washington [US], November 19 (ANI): The US Food and Drug Administration on Friday (local time) expanded the emergency use authorization (EUA) for the Pfizer and Moderna COVID-19 vaccine boosters signaling that the shots can be given to anyone aged 18+ at least six months after completion of
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