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FDA Appoints Biotech Executive as Top Drug Regulator

Associated Press News on MSN · 9h

FDA names former pharmaceutical company executive to oversee US drug program

The Food and Drug Administration named a longtime pharmaceutical executive to run the agency’s drug program. Dr.

Bloomberg on MSN · 10h

FDA Appoints Biotech Executive as Top Drug Regulator Under RFK Jr.

Food and Drug Administration commissioner Marty Makary has chosen former biotech executive George Tidmarsh as the agency’s top drug regulator, the agency confirmed Monday.

UPI on MSN · 8h

Biotech exec George Tidmarsh picked as FDA's chief drug regulator

The U.S. Food and Drug Administration named ex-biotech exec George Tidmarsh as its chief drug regulator. FDA Commissioner Marty Makary called Tidmarsh an "accomplished physician-scientist and leader."

FDA suspends muscular dystrophy drug

Newsweek on MSN · 22h

FDA Suspends Muscular Dystrophy Drug After 3 Patient Deaths

The U.S. Food and Drug Administration ( FDA) has placed an immediate clinical hold on Sarepta Therapeutics' investigational gene therapy trials for limb girdle muscular dystrophy following three patient deaths potentially linked to the company's treatments.

InvestorsHub on MSN · 11h

Sarepta Shares Drop as FDA Suspends Gene Therapy Trials for Muscular Dystrophy

Shares of Sarepta Therapeutics Inc (NASDAQ:SRPT) plunged 10% after the company disclosed that the U.S. Food and Drug Administration (FDA) has imposed a clinical hold on several of its gene therapy programs targeting limb girdle muscular dystrophy (LGMD).

MarketWatch · 13h

FDA Places Sarepta's Investigational Gene-Therapy Trials on Hold Following Patient Death

The Food and Drug Administration placed a clinical hold on Sarepta Therapeutics' investigational gene-therapy clinical trials for limb-girdle muscular dystrophy, a group of genetic disorders that cause muscles to weaken and atrophy.

FDA recalls over 67,000 cases of Power Stick deodorant

Austin American-Statesman on … · 13h

FDA recalls over 67,000 cases of Power Stick deodorant due to manufacturing violations

On July 10, Pennsylvania-based health and beauty manufacturer A.P. Deauville announced a recall of 67,214 cases of its Power Stick roll-on deodorant due to violations of Current Good Manufacturing Practice (CGMP) standards, a set of FDA-enforced guidelines designed to ensure product safety and quality.

TODAY on MSN · 6h

The FDA just recalled 67,000 cases of deodorant — here’s what you need to know

But one thing we’re confident about is that nobody wants to use a deodorant that has been recalled, which is why we are sharing this news: The Food and Drug Administration has issued a recall on 67,000 cases of Power Stick antiperspirant deodorant.

MLive · 6h

Here’s what you should know about the 67,000 cases of deodorant being recalled

The FDA did not provide a reason for the recall, but said the products had a cGMP (Current Good Manufacturing Practices) deviation.

10hon MSN

FDA issues highest risk Warning for mushroom recall

Mushrooms sold across two states have been recalled over fears they could be harboring listeria, a bug that "can cause ...

FDA Approves Prefilled Syringe Presentation for Shingles Vaccine

Prefilled syringe eliminates the need to reconstitute separate vials prior to administration and simplifies the vaccine ...

STAT5h

New head of FDA drug center is a biotech veteran and an outspoken critic of the academic establishment

The Food and Drug Administration on Monday named George Tidmarsh, a longtime biotech executive who has a background in ...

2hon MSN

FDA panel promotes misinformation on antidepressants during pregnancy, psychiatrists say

A Food and Drug Administration panel on Monday discussing the use of antidepressants during pregnancy largely amounted to ...

11h

FDA Elevates Dubai Chocolate Spread Recall to Class 1 Over Salmonella Risk

Salmonella can cause serious and potentially fatal infections in young children, the frail or elderly, and others with ...

2hon MSN

FDA Announces Massive Ice Cream Recall in 23 States

The Food and Drug Administration (FDA) makes sure to stay on top and notify people whenever a recall is put into place.

13hon MSN

FDA Greenlights Game-Changing UV Technology That Could Make Raw Milk Safer to Consume

Tamarack Biotics’ TruActive process targets pathogens with UV light while keeping the milk’s enzymes and proteins intact.

Las Vegas Sun1d

Juul’s FDA approval doesn’t clear fog of e-cigarette risks, especially for teens

The Food and Drug Administration has granted permission for Juul to continue selling its e-cigarettes, offering some reprieve ...

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FDA Appoints Biotech Executive as Top Drug Regulator

FDA suspends muscular dystrophy drug

FDA recalls over 67,000 cases of Power Stick deodorant

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