ISO 10993-16:2017
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Évaluation biologique des dispositifs médicaux — Partie 16: Conception des études toxicocinétiques des produits de dégradation et des substances relargables
| Published By | Publication Date | Number of Pages |
| ISO | 2017-05 | 22 |
ISO 10993-16:2017 énonce les principes de conception et de mise en ?uvre des études toxicocinétiques relatives aux dispositifs médicaux. L'Annexe A décrit les considérations relatives à l'inclusion d'études toxicocinétiques dans l'évaluation biologique des dispositifs médicaux.
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