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Etiquetas: 7 febrero 2007, 7/02/2007, Acción farmacológica, Agencia Europea de Medicamentos, Autorización de comercialización, Bruselas, Células animales, Células humanas, Citoblastos embrionarios, Comisión de Asuntos Jurídicos, Comisión de Medio Ambiente, Comité de terapias avanzadas, Consejo sobre medicamentos de terapia avanzada, Directiva, Donante, EMEA, Enfermedades humanas, Enmiendas, Evaluación de datos, Fabricación, Farmacovigilancia, Funciones fisiológicas, Genoterapia, Hiltrud Breyer, Incentivos, informe, Ingeniería tisular, Inmunológica, Medicamentos biológicos, Medicamentos de terapia avanzada, Medicamentos para uso humano, Medicos, Metabólica, Miroslav Mikolášik, pacientes, Parlamento Europeo, Pequeñas y medianas empresas, Prevenir, Prevenir enfermedades humanas, Producto sanitario, PYME, Receptor, Reglamentación de los medicamentos, salud, Salud pública, Sanidad, Seguridad Alimentaria, Tejidos, Terapia celular somática, Tratado CE, Tratar.
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