News

Lab-grown salmon receives FDA approval
The cell-grown fish from Wildtype, which will be available in a fine-dining restaurant, marks the first time cultivated ...
GlobalData on MSN15h
FDA clears Neurent Medical’s NEUROMARK for chronic rhinitis treatment
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Neurent Medical's NEUROMARK system for the ...
Medscape15h
FDA Approves Triple Rx for Hypertension
The FDA has approved Widaplik, a triple-drug combination, for the treatment of hypertension in adults.
Investing.com France7h
La FDA approuve ZUSDURI d’UroGen pour le traitement du cancer de la vessie
PRINCETON, N.J. - La Food and Drug Administration américaine a approuvé ZUSDURI (mitomycine) pour le traitement des adultes ...
Investing.com France12h
La FDA approuve les gouttes oculaires de prednisolone acétate d’Amneal, lancement prévu pour le T3
BRIDGEWATER, N.J. - Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) a reçu l’approbation de la Food and Drug Administration américaine pour sa suspension ophtalmique de prednisolone acétate à 1% stérile, ...
Local health experts weigh in on recent COVID-19 vaccine recommendation changes
On Tuesday, the Food and Drug Administration (FDA) modified its existing standards surrounding the COVID-19 vaccine. ...
CNN3mon
FDA delays when a final rule on what foods can be labeled as ‘healthy’ goes into effect
“In accordance with this direction, FDA is delaying the effective date of the final rule ‘Food Labeling: Nutrient Content Claims; Definition of Term “Healthy”’ (89 FR 106064), until ...
Safe Group annonce l’obtention du 510(k) de la FDA pour la solution Frida de SpineUp
Safe Group annonce l’obtention du 510(k) de la FDA pour la solution Frida de SpineUp Fleurieux-sur-l’Arbresle - France - le 5 juin 2025 à 18h. Safe Group, acteur de référence dans le domaine des dispo ...
AFP13d
FDA Grants De Novo Clearance for Reflow Medical's Spur® Peripheral Retrievable Stent System
Reflow Medical, Inc., a leading developer of innovative medical devices focused on complex cardiovascular disease, announced ...
Hosted on MSN19d
FDA issues warning about allergy medications
Hundreds of people who stopped using allergy medications like Zyrtec and Xyzal noticed an uncomfortable new side effect, the U.S. Food and Drug Administration said in a warning issued this month ...
Medscape3mon
Dupilumab Under FDA Priority Review for Bullous Pemphigoid
Dupilumab has been accepted for priority review by the US Food and Drug Administration (FDA) for the treatment of bullous pemphigoid (BP) in adults, according to a press release from the ...
AFP14d
La FDA (Food and Drug Administration américaine) accorde la désignation d'interchangeabilité à la solution injectable HADLIMA™ (adalimumab-bwwd) de Samsung Bioepis et Organon
Paris (AFP) | 02/06/2025 - 15:00:21 | Présidentielle/Pologne: Macron appelle Nawrocki à continuer à bâtir une Europe "respectueuse de l'Etat de droit" Londres (AFP) | 02/06/2025 - 15:31:37 | Le printe ...