Drug Administration

U.S Food & Drugs Administration (FDA) shares a few key safety tips to handle a microwave at home. These tips can help prevent mishaps and let you enjoy the benefits of this useful invention.

Amid rising COVID-19 cases in China, the US Food and Drug Administration (FDA) released a list of hand sanitisers it recommends avoiding.

Ozempic, an injection that keeps blood sugar levels in check for patients with type 2 diabetes, has been in shortage for about four months, according to the database maintained by the US Food and Drug Administration.

LASIK - Laser-Assisted In Situ Keratomileusis - is the most commonly performed laser refractive surgery used to correct common vision problems. However, the surgery is now under the lens of the US Food and Drug Administration (FDA).

Neuralink is expected to begin human trials in six months, Elon Musk said on Wednesday. The brain chip interface is running behind schedule, and is said to have repeatedly missed internal deadlines to gain US Food and Drug Administration (FDA) approval to start human trials. Over a year ago, Neuralink demonstrated its technology on a monkey with a ...

The Maharashtra Food & Drug Administration (FDA) has asked all drug controller authorities in the country to stop the use of a particular batch of drug INJ OROFER FCM following the death of a patient at a Mumbai hospital.

Aurobindo Pharma units are recalling different products in the US market for manufacturing lapses, as per the US health regulator.

Maharashtra's Food and Drugs Administration has cancelled the baby powder manufacturing licence of Johnson & Johnson Pvt Ltd "in the interest of public health at large."

Maharashtra's Food and Drugs Administration (FDA) on Friday cancelled the baby powder manufacturing licence of Johnson & Johnson Pvt Ltd "in the interest of public health at large".

Maharashtra's Food and Drugs Administration (FDA) on Friday cancelled the baby powder manufacturing licence of Johnson & Johnson Pvt Ltd "in the interest of public health at large".

Lupin on Monday said it has received a tentative approval from the US health regulator to market Dasatinib tablets, used to treat certain types of cancer, in America.

US senators seek answers from Facebook, Instagram parent Meta regarding censored information on abortion posts. The senators questioned how many posts about abortion have been removed since the US Supreme Court overturned a long-standing right to such medical care. Meta, referring to a tweet by spokesman Andy Stone, stated that attempts to provide ...

The US Food and Drug Administration has ordered all vaping products produced by Juul Labs off the market after finding the former industry leader had failed to address certain safety concerns. Juul was blamed for a surge in youth vaping over its marketing of fruit and candy flavored e-cigarettes.

The US Food and Drug Administration granted emergency authorization Friday for the use of Pfizer and Moderna Covid-19 vaccines in the youngest children, the final age group awaiting immunization in most countries.

A panel of experts convened by the US Food and Drug Administration unanimously recommended Covid-19 vaccines Wednesday for children under five, the final age group awaiting immunization in most countries.

U.S Food & Drugs Administration (FDA) shares a few key safety tips to handle a microwave at home. These tips can help prevent mishaps and let you enjoy the benefits of this useful invention.

Amid rising COVID-19 cases in China, the US Food and Drug Administration (FDA) released a list of hand sanitisers it recommends avoiding.

Ozempic, an injection that keeps blood sugar levels in check for patients with type 2 diabetes, has been in shortage for about four months, according to the database maintained by the US Food and Drug Administration.

LASIK - Laser-Assisted In Situ Keratomileusis - is the most commonly performed laser refractive surgery used to correct common vision problems. However, the surgery is now under the lens of the US Food and Drug Administration (FDA).

Neuralink is expected to begin human trials in six months, Elon Musk said on Wednesday. The brain chip interface is running behind schedule, and is said to have repeatedly missed internal deadlines to gain US Food and Drug Administration (FDA) approval to start human trials. Over a year ago, Neuralink demonstrated its technology on a monkey with a ...

The Maharashtra Food & Drug Administration (FDA) has asked all drug controller authorities in the country to stop the use of a particular batch of drug INJ OROFER FCM following the death of a patient at a Mumbai hospital.

Aurobindo Pharma units are recalling different products in the US market for manufacturing lapses, as per the US health regulator.

Maharashtra's Food and Drugs Administration has cancelled the baby powder manufacturing licence of Johnson & Johnson Pvt Ltd "in the interest of public health at large."

Maharashtra's Food and Drugs Administration (FDA) on Friday cancelled the baby powder manufacturing licence of Johnson & Johnson Pvt Ltd "in the interest of public health at large".

Maharashtra's Food and Drugs Administration (FDA) on Friday cancelled the baby powder manufacturing licence of Johnson & Johnson Pvt Ltd "in the interest of public health at large".

Lupin on Monday said it has received a tentative approval from the US health regulator to market Dasatinib tablets, used to treat certain types of cancer, in America.

US senators seek answers from Facebook, Instagram parent Meta regarding censored information on abortion posts. The senators questioned how many posts about abortion have been removed since the US Supreme Court overturned a long-standing right to such medical care. Meta, referring to a tweet by spokesman Andy Stone, stated that attempts to provide ...

The US Food and Drug Administration has ordered all vaping products produced by Juul Labs off the market after finding the former industry leader had failed to address certain safety concerns. Juul was blamed for a surge in youth vaping over its marketing of fruit and candy flavored e-cigarettes.

The US Food and Drug Administration granted emergency authorization Friday for the use of Pfizer and Moderna Covid-19 vaccines in the youngest children, the final age group awaiting immunization in most countries.

A panel of experts convened by the US Food and Drug Administration unanimously recommended Covid-19 vaccines Wednesday for children under five, the final age group awaiting immunization in most countries.