Comunicados de prensa U.S. FDA Salud y ciencias de la vida — Feed RSS y monitoreo en vivo
PPN World sigue el feed RSS de U.S. FDA en tiempo real — 10 comunicados indexados en los últimos 30 días, el más reciente llegó hace 3 d. Síguelo con alertas de búsquedas guardadas, resúmenes con IA y búsqueda de texto completo.
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U.S. FDA forma parte de los más de 1,400 feeds de comunicados que PPN World monitorea de forma continua — una fuente en inglés centrada en el sector Salud y ciencias de la vida, clasificada bajo «Estados Unidos» en nuestro índice por país. Cada comunicado se deduplica, se geolocaliza y se enriquece con un resumen de IA, y puedes añadir alertas de búsquedas guardadas sobre cualquier palabra clave que publique. En los últimos 30 días, U.S. FDA ha publicado 10 comunicados, sobre todo los lunes, con cobertura reciente centrada en fda-approval, fda, lawsuit.
Sigue U.S. FDA en tiempo real en PPN World
Cada comunicado de U.S. FDA llega al cockpit segundos después de publicarse — deduplicado, clasificado, con alertas de búsquedas guardadas y resúmenes con IA, junto a más de 1,400 feeds.
Suscribirse →Últimos comunicados de U.S. FDA
- FDA Seeks Public Input to Support Ibogaine Researchhace 3 d
The U.S. Food and Drug Administration today announced a request for information (RFI) describing approaches the agency is considering for the design of early-phase clinical trials of ibogaine drug pro…
- FDA Approves First Heart Valve Designed to Grow with Childrenhace 7 d
The U.S. Food and Drug Administration today approved the Autus Size-Adjustable Valve, a surgically implanted pulmonary heart valve for pediatric patients with congenital pulmonary valve disease.
- FDA Launches Nationwide Effort to Expand Scientific Expertise and Consumer Voices to Advisory Committeeshace 8 d
The U.S. Food and Drug Administration today announced a broad, nationwide recruitment effort to expand the range of qualified voices and perspectives on its advisory committees— the independent bodies…
- FDA Investigation Leads to Charges Against Two Indian Nationals Involved in Transnational Counterfeit Drug Distribution Schemehace 9 d
The U.S. Attorney’s Office for the Middle District of Florida and the Criminal Division of the U.S. Department of Justice today announced federal charges against Swapnadip Roy, 33, and Vicky Ramancha,…
- FDA Approves First Treatment for MCT8 Deficiencyhace 10 d
The U.S. Food and Drug Administration today approved Emcitate (tiratricol) tablets for oral suspension to treat peripheral thyrotoxicosis (excess thyroid hormone levels in the blood that causes sympto…
- FDA intends to evaluate changes to the PMTA regulatory frameworkhace 10 d
FDA is carefully reviewing its experience implementing the Premarket Tobacco Product Application (PMTA) rule, as well as recent judicial developments, including a federal lawsuit filed in the U.S. Dis…
- Federal Court Enters Consent Decree Against Gold Star Distribution, Inc. Following Persistent Insanitary Warehouse Conditionshace 15 d
A U.S. Food and Drug Administration investigation resulted in a federal court order, dated Sept. 21, 2026, stopping a warehouse operator from distributing FDA-regulated products including food, drugs,…
- FDA Updates Regulations to Advance Innovative Alternatives to Animal Testinghace 17 d
The FDA today issued a direct final rule that updates its regulations to clarify that non-animal methods can be used where appropriate for testing the safety of drugs and biological products intended…
- FDA Approves First Gene Therapy for Pediatric Patients with Sanfilippo Syndrome Type Ahace 21 d
The U.S. Food and Drug Administration today approved Fayuvi (rebisufligene etisparvovec-hopf), the first treatment for pediatric patients with mucopolysaccharidosis type IIIA (MPS IIIA), also known as…
- FDA Launches Expedited IND Pilot, Begins Accepting Applicationshace 23 d
The U.S. Food and Drug Administration today announced the final design of the Expedited Investigational New Drug (IND) Pilot.
- FDA Takes Steps to Maintain Newborn Access to Life-Saving Starter Nutrition Productshace 34 d
The U.S. Food and Drug Administration today announced it is taking action, consistent with the Trump administration’s commitment to protecting vulnerable patients and maintaining access to critical me…
- FDA Grants Accelerated Approval to a New Breast Cancer Treatmenthace 34 d
The U.S. Food and Drug Administration today expanded treatment options for adult patients with advanced breast cancer, reflecting the FDA’s commitment to advancing medical innovation and getting new t…
Los comunicados más recientes de esta fuente se transmiten en vivo para los miembros de PPN World.