Fda

With Neuralink’s device, a robot surgically inserts a device into the brain that can then decode some brain activity and connect the brain signals to computers and other machines. A person paralyzed from the neck down, for example, could use the interface to manipulate her physical environment, as well as to write and communicate.

Elon Musk's Neuralink received approval last week from the US Food and Drug Administration to conduct human clinical trials, which one former FDA official called "really a big deal."

Elon Musk's brain-implant company Neuralink on Thursday said the US Food and Drug Administration (FDA) had given the green light to its first-in-human clinical trial, a critical milestone after earlier struggles to gain approval.

Zydus Lifesciences on Thursday said it received final approval from the US Food and Drug Administration (FDA) to manufacture and market Metoprolol Tartrate tablets in dosages of 25 mg, 50 mg, and 100 mg

Neuralink, Elon Musk's brain implant company, is said to have approached one of the biggest US neurosurgery centres ahead of the company's plans to launch a human clinical trial for its devices that have been in development since 2016. The firm is working to address concerns expressed by the US Food and Drug Administration after it rejected an appl...

Apple is reportedly planning to bring health features to the AirPods product line, but not before 2025. According to Bloomberg;s Mark Gurman, the tech giant is likely to add hearing-based health features to the AirPods including, “the ability to get hearing data of some sort," within the next two years.

Alembic Pharmaceuticals has received an approval from the US Food & Drug Administration to market Brexpiprazole tablets in strengths of 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg and 4 mg.

The US Food and Drug Administration said that more than 25,000 cases of the glass bottles have been recalled.

Global Pharma Healthcare, the drug manufacturer at the centre of the controversy, has said it's working closely with the US Food and Drug Administration (FDA).

The US Centers for Disease Control and Prevention (CDC) said it is testing unopened bottles of EzriCare Artificial Tears eye drops, manufactured by Chennai-based Global Pharma Healthcare.

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.

As per foodallergyawareness.org, sesame is an allergen, just like tree nuts milk etc. Read on to know more about sesame allergy.

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).

The import alert means all future shipments of products made at Halol can be refused admission to the US market until the facility becomes compliant with the FDA's Current Good Manufacturing Practice standards,

With Neuralink’s device, a robot surgically inserts a device into the brain that can then decode some brain activity and connect the brain signals to computers and other machines. A person paralyzed from the neck down, for example, could use the interface to manipulate her physical environment, as well as to write and communicate.

Elon Musk's Neuralink received approval last week from the US Food and Drug Administration to conduct human clinical trials, which one former FDA official called "really a big deal."

Elon Musk's brain-implant company Neuralink on Thursday said the US Food and Drug Administration (FDA) had given the green light to its first-in-human clinical trial, a critical milestone after earlier struggles to gain approval.

Zydus Lifesciences on Thursday said it received final approval from the US Food and Drug Administration (FDA) to manufacture and market Metoprolol Tartrate tablets in dosages of 25 mg, 50 mg, and 100 mg

Neuralink, Elon Musk's brain implant company, is said to have approached one of the biggest US neurosurgery centres ahead of the company's plans to launch a human clinical trial for its devices that have been in development since 2016. The firm is working to address concerns expressed by the US Food and Drug Administration after it rejected an appl...

Apple is reportedly planning to bring health features to the AirPods product line, but not before 2025. According to Bloomberg;s Mark Gurman, the tech giant is likely to add hearing-based health features to the AirPods including, “the ability to get hearing data of some sort," within the next two years.

Alembic Pharmaceuticals has received an approval from the US Food & Drug Administration to market Brexpiprazole tablets in strengths of 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg and 4 mg.

The US Food and Drug Administration said that more than 25,000 cases of the glass bottles have been recalled.

Global Pharma Healthcare, the drug manufacturer at the centre of the controversy, has said it's working closely with the US Food and Drug Administration (FDA).

The US Centers for Disease Control and Prevention (CDC) said it is testing unopened bottles of EzriCare Artificial Tears eye drops, manufactured by Chennai-based Global Pharma Healthcare.

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.

As per foodallergyawareness.org, sesame is an allergen, just like tree nuts milk etc. Read on to know more about sesame allergy.

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).

The import alert means all future shipments of products made at Halol can be refused admission to the US market until the facility becomes compliant with the FDA's Current Good Manufacturing Practice standards,