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The U.S. Senate passed the FDA Modernization Act 3.0 to advance human-relevant drug testing methods, reducing animal use and speeding development.
The U.S. Senate passed the FDA Modernization Act 3.0, advancing new approach methodologies (NAMs) like human cell-based and in silico models to modernize drug testing.
The law directs the FDA to establish qualification pathways for these methods, aiming to improve accuracy, reduce animal use, and shorten development times.
DiNABIOS, a Swiss life science company, welcomed the move as a major step toward more ethical, efficient, and human-relevant research, emphasizing the need for scientific rigor and reproducibility in adopting these technologies.
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El Senado de los Estados Unidos aprobó la Ley de Modernización de la FDA 3.0 para avanzar en los métodos de prueba de fármacos relevantes para humanos, reduciendo el uso de animales y acelerando el desarrollo.