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Etiquetas: 2007, Acuerdo sobre los Aspectos de los Derechos de Propiedad Intelectual relacionados con el Comercio, ADPIC, AEM, AESEG, Agencia Española del Medicamento, Antonio Iñesta García, Asociación Española de Fabricantes de Genéricos, Bibliografía, Biogenéricos, Certificado complementario de protección de la patente, Conclusiones y propuestas, Convenio de la Patente Europea, CPE, Déficit de transparencia de información, Disposición Bolar, Doctor en Farmacia, EMEA, España, European Medicines Agency, Evolución de los genéricos en España, Fundación Alternativas, genéricos, Genéricos de productos biológicos, Gráficos y Cuadros, Legislación que afecta a los genéricos, Ley de garantías, Madrid, Ministerio de Sanidad y Consumo, MSC, PP, Prescripción, Prescripción de genéricos, Prescripción por principio activo, PRG, Protección de patente, protección de registro, Resumen ejecutivo, salud, Sanidad, Siglas, Sistema Nacional de Salud, Situación y consumo de genéricos en países de EEUU y Canadá, Situación y consumo de genéricos en países de la UE, Tablas, UE, Unión Europea, Uso racional de los medicamentos, Uso racional de los medicamentos y productos sanitarios.