Il progresso scientifico e tecnologico applicato allo sviluppo dei prodotti medicinali pone nuove sfide al mondo regolatorio rendendo necessari approcci che consentano di rispondere a queste rinnovate esigenze. Il fine ultimo è quello di garantire ai pazienti un accesso tempestivo alle innovazioni tecnologiche, nel rispetto dei compiti regolatori affidati ad AIFA a tutela della salute …
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