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Adulterated Drugs On Decline Amid Crackdown

Rise in raids on illicit drug manufacturing units, alongside arrests for the production, sale, or distribution of spurious or adulterated drugs. Photograph: Yves Herman/Reuters The......

US FDA warns against side effects of malaria drug

The United States Food and Drug Administration has issued a safety communication regarding the known side effects of anti-malarial drug hydroxychloroquine, touted by President Donald Trump for......

FDA to prosecute Cadbury for insect infestations

A lab report on "insect infestations" in a Cadbury chocolate bar has come out positive, the Maharashtra Food and Drugs Administration said on Monday The report was positive for the presence of two......

US authorises Moderna vaccine for emergency use

Moderna has become the second company to get emergency use authorisation for its anti-coronavirus vaccine from the United States Food and Drug Administration (FDA), a week after the one developed......

US authorizes Pfizer's COVID vaccine for emergency use

The United States Food and Drug Administration authorised Pfizer's Covid-19 vaccine for emergency use for the prevention of coronavirus disease in individuals 16 years of age and older. IMAGE: A......

After J&J, FDA puts Wipro on notice

The Maharashtra Food and Drug Adminstration has served a notice to Wipro for allegedly "misbranding and mislabelling" its baby oil. "We have served notice to Wipro for misbranding and labelling......

FDA asks Wockhardt to conduct global assessment of its plants

Indian generic drug manufacturer Wockhardt has been asked by America's Federal Drug Administration to conduct a global assessment of its plants to ensure that the drug produced by the company......

After Ranbaxy, US FDA turns the heat on Actavis

The US Congressional committee, which is inquiring into the country's Food and Drug Administration's handling of drug-marketing approvals of India's leading drug-maker Ranbaxy, has extended its......

Maharashtra FDA raps Subhiksha

The Maharashtra Food and Drug Administrationhas suspended the licence of Subhiksha Trading Services,warehousing subsidiary of food and grocery retailer Subhiksha, for 20 days. The regulator said......

'Red Bull' under FDA lens

Maharashtra Food and Drug Administration has prohibited the sales of 'Red Bull', an energy drink, following complaints that the product's main ingredient Taurine is an animal derivative, which the......

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Fda Commissioner

News for Fda Commissioner

Adulterated Drugs On Decline Amid Crackdown

US FDA warns against side effects of malaria drug

FDA to prosecute Cadbury for insect infestations

US authorises Moderna vaccine for emergency use

US authorizes Pfizer's COVID vaccine for emergency use

After J&J, FDA puts Wipro on notice

FDA asks Wockhardt to conduct global assessment of its plants

After Ranbaxy, US FDA turns the heat on Actavis

Maharashtra FDA raps Subhiksha

'Red Bull' under FDA lens

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