FDA

Dec 10, 2023
In the last week’s press release, the U.S. Food and Drug Administration (FDA) has approved two groundbreaking gene therapies- Casgevy and Lyfgenia for sickle cell disease (SCD) treatment.
 - Sakshi Post
Sep 20, 2023
San Francisco, Sep 20 (IANS) Elon Musk-owned brain computer interface company Neuralink is now recruiting its first test subjects for human trials to help those with paralysis control devices.
US FDA Authorises First Oral Antiviral For Treatment Of COVID - Sakshi Post
Dec 23, 2021
The US Food and Drug Administration has granted Pfizer's Paxlovid an emergency use authorization for the treatment of COVID-19 in adults and children (12 years of age and older).
 - Sakshi Post
Jun 29, 2021
New Delhi: Moderna Inc, an American pharmaceutical firm, applied to the Drugs Controller General of India (DGCI) on Tuesday to utilise its Covid vaccine for emergency use in anyone aged 18 and up,...
 - Sakshi Post
Aug 24, 2020
The US Food and Drug Administration issued an emergency approval for the use of convalescent plasma as a treatment against COVID-19 that killed more than 1,76,000 people in the US.
Representational Image - Sakshi Post
Nov 09, 2018
The U.S. Food and Drug Administration plans to require strict limits on the sale of most flavored e-cigarettes, including age verification controls for online sales, in an effort to curtail their use...
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