US FOOD AND DRUG ADMINISTRATION

A conservative federal judge in Texas heard arguments Wednesday from a Christian group seeking to overturn the Food and Drug Administration’s more than 2-decade-old approval of an abortion medication, in a case that could threaten the most common fo...

The US Food Drug and Administration (USFDA) concluded that the inspection classification of Aurobindo Pharma's wholly owned subsidiary, APL Healthcare's facility of telangana is Volunatry Action Indicated (VAI).Aurobindo Pharma gets VAI classificati...

The U.S. moved a step closer to expanding COVID-19 vaccinations for millions more children as government advisers on Tuesday endorsed kid-size doses of Pfizer's shots for 5- to 11-year-olds. A Food and Drug Administration advisory panel voted unanim...

Bharat Biotech International Limited (BBIL) has conveyed to the government that it has already submitted 90 per cent of documents to WHO for obtaining emergency use listing (EUL) for the Covaxin vaccine, sources said on Monday.Bharat Biotech approac...

Pentagon to issue guidance to make vaccine mandatory for military now that Pfizer is approved by Food and Drug Administration. The U.S. gave full approval to Pfizer's COVID-19 vaccine Monday, a milestone that could lift public confidence in the shot...

US Government health officials on Monday approved the first new drug for Alzheimer's disease in nearly 20 years, disregarding warnings from independent advisers that the much-debated treatment hasn't been shown to help slow the brain-destroying dise...

Setback to Bharat Biotech's COVID-19 vaccine Covaxin, the US Food and Drug Administration has "recommended" Ocugen Inc, the US partner of the Indian vaccine maker, to go for Biologics Licence Application (BLA) route with additional data, nixinghopes...

The U.S. gave full approval to Pfizer's COVID-19 vaccine Monday, a milestone that could lift public confidence in the shots and spur more companies, universities and local governments to make vaccinations mandatory. The formula made by Pfizer and it...

Lucknow: In yet another setback for the Bharatiya Janata Party (BJP), Uttar Pradesh minister Dharam Singh Saini resigned from the ruling party on Thursday. Dharam Singh Saini was the Minister of State (Independent Charge), Ayush, Food Security and D...

Washington: An expert committee convened by the US Food and Drug Administration voted heavily in favor of recommending the Pfizer-BioNTech Covid-19 vaccine for emergency use approval on Thursday.Pfizer covid vaccine gets US experts' nod for emergenc...

Reports of possible allergic reactions to the COVID-19 vaccines produced by Pfizer-BioNTech and Moderna, both recently approved for emergency use by the US Food and Drug Administration (FDA), have raised public concern. A team of experts led by alle...

Drug firm Aurobindo Pharma on Monday said the US health regulator has issued 9 observations after inspection of its unit 4 formulation facility in Hyderabad. The United States Food and Drug Administration (USFDA) has conducted an inspection at the c...

Drug maker Cipla Ltd on Friday got four observations from US Food and Drug Administration for three of its manufacturing units in Goa.Cipla gets 4 observations from USFDA for 3 Goa units

Watch brokerages view on Divi’s Lab that plunged 22 per cent on reports of strong observations made by the US Food and Drug Administration on its facility in Vishakhapatnam and Cipla, which received UK MHRA approval for gAdvair.Brokerages view about...

Drug firm Dr Reddy's Laboratories said it has received a warning letter from US health regulator over inadequate quality control procedures at its three drug manufacturing units in India. Check out the video for more information.Dr Reddy's gets FDA ...

Ipca Laboratories Ltd said it has temporarily suspended shipments to the United States from one of its drug ingredient manufacturing plants after the US Food and Drug Administration expressed concerns regarding the unit.Ipca stops API exports from R...

Lupin shares succumbed to extreme selling pressure after reports emerged that the company received Form 483 for its Mandideep plant in Goa from the US Drug and Food Agency (USFDA). The stock closed lower by 6.27 per cent.USFDA concerns hit Lupin; st...