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Les textes de référence pour les dispositifs médicaux et la matériovigilance incluent des directives européennes et des lois nationales, définissant les conditions de mise sur le marché, les exigences essentielles de sécurité, et les obligations de matériovigilance. Ces réglementations garantissent la sécurité et l'efficacité des dispositifs médicaux, tout en encadrant la publicité et la revente. Les obligations des intervenants en matériovigilance sont cruciales pour la gestion des incidents.
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