Us Health Regulators
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Is Titanium Dioxide Safe? Skittles Pulls Ingredient After Health Warnings
Though titanium dioxide was never banned by US regulators, the additive has long been under scrutiny for potential health risks.
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What Happens To Our Body When We Consume Sugary Drinks, Health Expert Simplifies
Are you consuming excessive sugary drinks without realising their health impact on your body? A wellness expert has simplified the process to help us make healthier dietary choices.
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Elon Musk's Neuralink Gets Go Ahead For Brain Chip Implant In 2nd Patient: Report
The US health regulator has allowed billionaire Elon Musk's Neuralink to implant its brain chip in a second person after it proposed to fix a problem that occurred in its first patient, the Wall Street Journal reported on Monday.
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Biden Strengthens US Air Quality Regulations, Angering Industry Groups
President Joe Biden's administration on Wednesday announced tough new air quality standards it said were sorely needed to protect the health of vulnerable communities, though industry groups have said the move would devastate domestic manufacturing.
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US Makes New Alzheimer's Drug More Widely Accessible
The US drug regulator gave full approval to a new Alzheimer's medicine on Thursday, a move that makes it more widely available to the public through government-run health insurance for the elderly.
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Zydus Gets US Regulator's Approval To Market Generic Drug For Myxedema Coma
Zydus Lifesciences today said it has received approval from the US health regulator to market a generic product which is used to treat myxedema coma.
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US Health Regulator Lists 378 Hand Sanitisers Consumers Should Not Use
Amid rising COVID-19 cases in China, the US Food and Drug Administration (FDA) released a list of hand sanitisers it recommends avoiding.
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"Drug Products Adulterated": US Regulator Warns Sun Pharma's Gujarat Plant
The US health regulator has pulled up drug major Sun Pharma for manufacturing lapses, including failure to follow appropriate written procedures designed to prevent microbiological contamination of drug products, at its Gujarat-based plant.
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LASIK Patients Should Be Warned of Risks Before Eye Procedure, Says US Health Regulator
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).
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Pharma Firm Lupin Gets US Regulator Nod For Generic Drug To Treat Cancer
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.
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Pharma Firm Lupin Gets US Regulator Nod For Generic Drug To Treat Seizures
Pharmaceuticals firm Lupin Ltd on Thursday said it has received approval from the US health regulator to market its generic rufinamide tablets used in the treatment seizures.
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US Regulator to Investigate Deaths of Amazon Workers in New Jersey: Details
US Occupational Health and Safety Administration (OSHA) investigators are probing the death of an Amazon worker, along with an injury that potentially led to the death of another employee. The US work-safety regulator is already probing a fatality during the company's annual Prime Day shopping event in mid-July, and all three deaths occurred within...
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US Health Regulator Lifts Hold On Covaxin's Clinical Trials
The US Food and Drug Administration which has put on hold phase 2/ 3 clinical trials of Bharat Biotech's COVID-19 vaccine Covaxin, in USA, has lifted pause, according to a statement issued by Ocugen Inc, Bharat Biotech's partner for jab in US, Canada
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Glenmark Pharmaceuticals Gets Final US Approval For Lacosamide Tablet
Homegrown pharma major Glenmark Pharmaceuticals Ltd on Monday said it has received final approval from the US health regulator for its generic Lacosamide tablet, indicated for prevention and control of seizures.
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US Health Regulator Clears Covaxin For Clinical Trials In Adults In America
Bharat Biotech's COVID-19 vaccine Covaxin has been given clearance for clinical trials in adults by the US Food and Drug Administration (FDA).
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Is Titanium Dioxide Safe? Skittles Pulls Ingredient After Health Warnings
Though titanium dioxide was never banned by US regulators, the additive has long been under scrutiny for potential health risks.
-
What Happens To Our Body When We Consume Sugary Drinks, Health Expert Simplifies
Are you consuming excessive sugary drinks without realising their health impact on your body? A wellness expert has simplified the process to help us make healthier dietary choices.
-
Elon Musk's Neuralink Gets Go Ahead For Brain Chip Implant In 2nd Patient: Report
The US health regulator has allowed billionaire Elon Musk's Neuralink to implant its brain chip in a second person after it proposed to fix a problem that occurred in its first patient, the Wall Street Journal reported on Monday.
-
Biden Strengthens US Air Quality Regulations, Angering Industry Groups
President Joe Biden's administration on Wednesday announced tough new air quality standards it said were sorely needed to protect the health of vulnerable communities, though industry groups have said the move would devastate domestic manufacturing.
-
US Makes New Alzheimer's Drug More Widely Accessible
The US drug regulator gave full approval to a new Alzheimer's medicine on Thursday, a move that makes it more widely available to the public through government-run health insurance for the elderly.
-
Zydus Gets US Regulator's Approval To Market Generic Drug For Myxedema Coma
Zydus Lifesciences today said it has received approval from the US health regulator to market a generic product which is used to treat myxedema coma.
-
US Health Regulator Lists 378 Hand Sanitisers Consumers Should Not Use
Amid rising COVID-19 cases in China, the US Food and Drug Administration (FDA) released a list of hand sanitisers it recommends avoiding.
-
"Drug Products Adulterated": US Regulator Warns Sun Pharma's Gujarat Plant
The US health regulator has pulled up drug major Sun Pharma for manufacturing lapses, including failure to follow appropriate written procedures designed to prevent microbiological contamination of drug products, at its Gujarat-based plant.
-
LASIK Patients Should Be Warned of Risks Before Eye Procedure, Says US Health Regulator
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).
-
Pharma Firm Lupin Gets US Regulator Nod For Generic Drug To Treat Cancer
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.
-
Pharma Firm Lupin Gets US Regulator Nod For Generic Drug To Treat Seizures
Pharmaceuticals firm Lupin Ltd on Thursday said it has received approval from the US health regulator to market its generic rufinamide tablets used in the treatment seizures.
-
US Regulator to Investigate Deaths of Amazon Workers in New Jersey: Details
US Occupational Health and Safety Administration (OSHA) investigators are probing the death of an Amazon worker, along with an injury that potentially led to the death of another employee. The US work-safety regulator is already probing a fatality during the company's annual Prime Day shopping event in mid-July, and all three deaths occurred within...
-
US Health Regulator Lifts Hold On Covaxin's Clinical Trials
The US Food and Drug Administration which has put on hold phase 2/ 3 clinical trials of Bharat Biotech's COVID-19 vaccine Covaxin, in USA, has lifted pause, according to a statement issued by Ocugen Inc, Bharat Biotech's partner for jab in US, Canada
-
Glenmark Pharmaceuticals Gets Final US Approval For Lacosamide Tablet
Homegrown pharma major Glenmark Pharmaceuticals Ltd on Monday said it has received final approval from the US health regulator for its generic Lacosamide tablet, indicated for prevention and control of seizures.
-
US Health Regulator Clears Covaxin For Clinical Trials In Adults In America
Bharat Biotech's COVID-19 vaccine Covaxin has been given clearance for clinical trials in adults by the US Food and Drug Administration (FDA).
