F.D.A. Expands Access to Clozapine, a Key Treatment for Schizophrenia
Federal regulators will no longer require patients to provide blood tests before receiving the drug from pharmacies.
Map Shows States With Listeria Cases as FDA Recalls Nutritional Shake
Use precise geolocation data and actively scan device characteristics for identification. This is done to store and access ...
Drug compounders sue over weight loss drugs’ removal from FDA shortage list
A trade group representing compounding pharmacies has filed a lawsuit against the Food and Drug Administration (FDA) for ...
Oops! Trump Accidentally Fired FDA Medical Device Reviewers
The Food and Drug Administration is scrambling to bring back hundreds of critical workers laid off en masse by DOGE.
Pixel Watch 3 gets FDA clearance for Loss of Pulse alerts
Google just announced it’s received FDA clearance for the Pixel Watch 3’s Loss of Pulse Detection feature. It will start ...
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FDA dings Piramal API plant with Form 483 detailing problems tied to quality control, equipment cleaning and more
Roughly a year after receiving an FDA reprimand at its manufacturing plant in Michigan, Indian drugmaker Piramal Pharma has ...
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Drug compounders sue FDA over Novo Nordisk’s Ozempic, Wegovy
Drug compounders aren’t ready to give up their ability to produce off-brand versions of Novo Nordisk’s weight-loss drug ...
Baby Food Recalled in 45 States as FDA Sets Highest Risk Level
The recall was first announce d on January 31, and the FDA released its Class I risk classification on February 25. It has raised concerns about infant product safety standards. The products were ...
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Emalex Heads to FDA After Phase III Tourette Syndrome Win
In the Phase III trial, 41.9% of pediatric Tourette syndrome patients relapsed after ecopipam treatment, as compared with ...
FDA delays when a final rule on what foods can be labeled as ‘healthy’ goes into effect
The FDA's new standards for foods before they can be labeled as "healthy" on their packaging will go into effect about two ...
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Nasal spray recalled nationwide; risk of infection: FDA
The U.S. Food & Drug Administration (FDA) has announced the voluntary recall of a sinus nasal wash bottle system following a ...
Opus Genetics gets FDA Fast Track designation for Phentolamine Ophthalmic Solution
Opus Genetics (IRD) said that the FDA has granted Fast Track designation for Phentolamine Ophthalmic Solution 0.75%, reported ...