avril 02, 2024
Le Rôle de la Gestion des Risques Biologiques dans le Développement des Dispositifs Médicaux
The biological evaluation of medical devices, guided by ISO standards, must be integrated into the risk management process to ensure comprehensive consideration of biological risks, a task often challenging for manufacturers but addressed by Qserve through expert collaboration, structured assessment, and data integration for enhanced safety evaluation and testing.
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