Search For "drug administration"
Third member of US FDA advisory panel resigns over Alzheimer's drug approv
Updated : 4 years, 9 months ago IST
Washington [US], June 11 (ANI): A third member of the US Food and Drug Administration (FDA) expert advisory panel resigned from the body after it approved a controversial Alzheimer's drug named Aduhelm recently.
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Bharat Biotech's US partner, Ocugen to apply for full approval for Covaxin
Updated : 4 years, 9 months ago IST
Pennsylvania [US], June 11 (ANI): Bharat Biotech's US partner Ocugen Inc said that the company will no longer pursue an Emergency Use Authorization (EUA) for COVAXIN and the US Food and Drug Administration (FDA) has recommended that the company go for the Biologics Licence Application (BL
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US FDA okays first new Alzheimer's drug in nearly 2 decades
Updated : 4 years, 9 months ago IST
Washington [US], June 8 (ANI): The United States Food and Drug Administration (FDA) has approved a new drug for Alzheimer's, the first new medicine against the disease in almost two decades.
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Glenmark Pharmaceuticals receives ANDA approval for Theophylline Extended-
Updated : 4 years, 9 months ago IST
Mumbai (Maharashtra) [India], June 4 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Theophylline Extended-release Tablets, 300 mg and 450 mg, bioequivalent and therapeutically equivalent
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As pressure mounts on China over COVID-19 origins, ex-FDA chief says 'lab
Updated : 4 years, 9 months ago IST
Washington [US], May 31 (ANI): Amid mounting concerns regarding a renewed probe of the origins of COVID-19 in China, former US Food and Drug Administration (FDA) Commissioner Scott Gottlieb said that accidental lab leaks 'happen all the time' and there have been six last known outbreaks of S
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Evidence of COVID-19 originating from Chinese lab continues to grow: Forme
Updated : 4 years, 9 months ago IST
Washington [China], May 25 (ANI): The former head of the US Food and Drug Administration (FDA) on Monday said that circumstantial evidence of COVID-19 originating in a lab in China's Wuhan continues to grow as researchers are yet to prove that the virus jumped from an animal to humans, The H
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Glenmark Pharmaceuticals receives ANDA approval for Icatibant Injection, 3
Updated : 4 years, 9 months ago IST
Mumbai (Maharashtra) [India], May 24 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Icatibant Injection, 30 mg/3 mL (10 mg/mL) Single-Dose Prefilled Syringe, the generic version of F
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US FDA approves emergency use of Pfizer-BioNTech vaccine for children in 1
Updated : 4 years, 10 months ago IST
Washington [US], May 11 (ANI): The US Food and Drug Administration (FDA) on Monday (local time) authorised the emergency use of the Pfizer-BioNTech COVID-19 vaccine to children in the age group of 12-15 years.
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COVID-19: Remdesivir Injection Monitoring Centre in Punjab to stop black
Updated : 4 years, 10 months ago IST
Chandigarh (Punjab) [India], May 9 (ANI): Punjab Food and Drug Administration has established the 'Remdesivir Injection Monitoring Centre' at the head office to stop black marketing of the anti-viral drug amid the COVID-19 pandemic.
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Pfizer, BioNTech seek full approval of COVID-19 vaccine across US
Updated : 4 years, 10 months ago IST
Washington [US], May 7 (ANI): Pharmaceutical giants Pfizer and BioNTech on Friday said that they have started the process for getting the US Food and Drug Administration (FDA) complete authorisation of its COVID-19 vaccine after having emergency use authorization for almost five months.
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US won't release AstraZeneca's COVID vaccine for export until sure about s
Updated : 4 years, 10 months ago IST
Washington [US], April 30 (ANI): The US Food and Drug Administration will not release AstraZeneca's coronavirus vaccine for export to other countries until it is sure the doses have been manufactured to US quality standards and will be safe and effective, a government official told CNN on Th
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Bangladesh approves emergency use of Russia's Sputnik V COVID-19 vaccine
Updated : 4 years, 10 months ago IST
Dhaka [Bangladesh], April 28 (ANI): The Directorate General of Drug Administration (DGDA) of Bangladesh has green-lit the emergency use of Russia's Sputnik V COVID-19 vaccine, the second vaccine to be used in the country.
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