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Etiquetas: 09/05/2013, 9 mayo 2013, Acontecimiento adverso grave, Borrador, Buena práctica clínica, Comités de ética, Consentimiento informado, Disposiciones generales, Ensayo clínico, Ensayos clínicos con medicamentos, Ensayos clínicos con menores, Ensayos clínicos con sujetos sin capacidad para otorgar su consentimiento informado, Ensayos clínicos sin beneficio directo para la salud de los sujetos, Financiación, Indemnización por daños y perjuicios, Inspección, Investigación biomédica, Investigación con medicamentos, Madrid, medicamentos, Protección de los sujetos del ensayo, R&D, Reacción adversa, Reall Decreto, Registro de estudios clínicos, salud, Sanidad, Suspensión.
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