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FDA Appoints Biotech Executive as Top Drug Regulator

Bloomberg on MSN · 1d

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.

Associated Press News on MSN · 1d

FDA names former pharmaceutical company executive to oversee US drug program

The Food and Drug Administration on Monday named a longtime pharmaceutical executive to run the agency’s drug program, the latest in a string of leadership changes at the agency. FDA Commissioner Marty Makary announced that Dr.

UPI on MSN · 1d

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."

Sarepta Therapeutics, FDA and gene

Associated Press News on MSN · 16h

Sarepta shares slide again as drugmaker bows to FDA pressure to pause gene therapy

Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that have attracted attention from regulators.

U.S. News & World Report · 1d

Children's Hospital LA Pauses Use of Sarepta Gene Therapy for All Patients

Children's Hospital Los Angeles, citing recent U.S. Food and Drug Administration actions, on Monday said it has paused usage of Sarepta Therapeutics' gene therapy Elevidys in all patients with muscular dystrophy.

MarketWatch · 20h

Sarepta Therapeutics’ stock slips further as company bows to FDA pressure to halt shipments

Sarepta Therapeutics shares traded lower in premarket trade on Tuesday, as the drugmaker relented to a Food and Drug Administration request to halt the shipments of a gene therapy.

10h

FDA Issues Recall in Various States Due to Possible Listeria Contamination

The Food and Drug Administration (FDA) has been busy lately with various recalls. One involved Power Stick deodorant and ...

19hon MSN

Replimune says FDA rejected its lead drug for skin cancer

Replimune (NASDAQ:REPL) announced on Tuesday that the U.S. Food and Drug Administration (FDA) issued a Complete Response ...

2don MSN

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 ...

American Hospital Association11h

Recall issued by FDA for certain craniotomy kits

The Food and Drug Administration has identified a Class I recall of certain lots of Medline Industries Craniotomy ...

7don MSN

FDA approves new blue food dye derived from gardenia fruit

The U.S. Food and Drug Administration approved a new blue color additive derived from the fruit of the gardenia, a flowering ...

Health and Me on MSN3d

"Obsolete And Unnecessary": FDA Set To Revoke 52 Nutrition And Labeling Rules

The FDA plans to revoke 52 outdated nutrition and labeling regulations to streamline food industry standards, citing them as ...

5don MSN

Juul can continue selling its tobacco and menthol e-cigarettes, FDA says

WASHINGTON (AP) — The Food and Drug Administration is allowing vaping brand Juul to keep its e-cigarettes on the market, ...

TAG24 on MSN5d

Food and Drug Administration may soon revise hormone replacement therapy warnings

US Food and Drug Administration Commissioner Marty Makary signaled Thursday that he is open to revising strict warning labels ...

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