Search For "us fda"
Know why EECP is an alternative to Bypass Surgery
Updated : 3 years, 9 months ago IST
Mumbai (Maharashtra) [India], June 24 (ANI/PNN): Enhanced External counterpulsation (EECP) is a US-FDA-approved treatment for patients with heart blockages exertion.
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Glenmark Pharmaceuticals receives sANDA approval for Abiraterone Acetate T
Updated : 3 years, 10 months ago IST
Mumbai (Maharashtra) [India], May 20 (ANI/PRNewswire): Glenmark Pharmaceuticals Inc, USA (Glenmark) has received final approval by the United States Food & Drug Administration (US FDA) for Abiraterone Acetate Tablets USP, 500 mg, the generic version of Zytiga®1 Tablets, 500 mg, of J
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NeoImmuneTech obtains approval for phase 2 trial of brain tumor treatment
Updated : 3 years, 10 months ago IST
Seoul [South Korea], May 12 (ANI/Global Economic): NeoImmuneTech said on the 11th that it has obtained the approval for a phase 2 clinical trial plan that concomitant administration of US Merck's immune checkpoint inhibitor Keytruda and its T-cell amplifier NT-I7 to patients with glioblastom
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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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US FDA clinical study proves non-contact thermometers fail to meet accurac
Updated : 4 years, 1 month ago IST
Watertown (Massachusetts) [US], February 15 (ANI/BusinessWire India): Since the start of the pandemic, non-contact infrared thermometers (NCITs) have been widely used as a screening method for fever detection in healthcare and public settings, as fever is a leading sign of COVID-19. Now, a n
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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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Philippines FDA approves world's first generic version of Pfizer's anti-Co
Updated : 4 years, 1 month ago IST
Manila [Philippines], January 26 (ANI/PNN): The Philippines Food and Drug Administration (FDA) has approved the world's first generic version of Pfizer's anti-Coronavirus pill Paxlovid, just days after the original was granted Emergency Use Authorisation (EUA) by the US FDA.
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Glenmark's subsidiary receives NDA Approval by US FDA for Ryaltris™
Updated : 4 years, 2 months ago IST
Mumbai (Maharashtra) [India], January 14 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited, a research-led, global integrated pharmaceutical company announced that its fully owned subsidiary Glenmark Specialty S.A. (Switzerland), received FDA approval on its New Drug Application (NDA) fo
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US FDA authorizes Pfizer's COVID antiviral pill for people aged 12
Updated : 4 years, 3 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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US formally recommends Pfizer COVID-19 vaccine for children aged 5-11
Updated : 4 years, 4 months ago IST
Washington [US], November 3 (ANI): Following rigorous review and authorization process by the US Food and Drug Administration (FDA), the Centers for Disease Control (CDC) on Tuesday (local time) has formally recommended the Pfizer COVID-19 vaccine for children 5-11.
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