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Informe sobre los aspectos científicos y jurídicos que avalan la necesidad de que los próximos anticuerpos monoclonales biosimilares cumplan directrices y procesos regulatorios específicos para asegurar su calidad, eficacia y seguridad
Etiquetas: 08/05/2014, 8 mayo 2014, Aniversario, Anticuerpos Clonales Biosimilares, Anticuerpos monoclonales, Anticuerpos monoclonales comercializados en España, Aplicaciones clínicas de los anticuerpos monoclonales, Estructura, Francisco Zaragozá, Generación de anticuerpos monoclonales humanos, Generación de moléculas recombinantes derivadas de anticuerpos monoclonales, informe, Instituto Roche, Julio Sánchez Fierro, Marco regulatorio, Mecanismos de acción de los anticuerpos monoclonales, Medidas para mejorar las características funcionales, Presente y futuro del desarrollo de anticuerpos monoclonales, Presente y futuro del Marco Regulatorio de los Anticuerpos Monoclonales Biosimilares, Roche, salud, Sanidad, Tecnologías para la generación de anticuerpos monoclonales, Valencia.
Etiquetas: 28 de septiembre de 2007, Agencia Europea del Medicamento, Aparición de los Medicamentos Biosimilares, Biosimilar frente a innovador, Biosimilares, Biotecnología, EMEA, Fármacos, Marco regulatorio, Medicamentos biotecnológicos, Revisión, salud, Sanidad, Una nueva realidad, Working Group on Biosimilars, Working Party on Biotechnology.
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