ISO/FDIS 10993-16Under development

Biological evaluation of medical devices — Part 16: Toxicokinetic evaluation for degradation products and leachables

Évaluation biologique des dispositifs médicaux — Partie 16: Évaluation toxicocinétique des produits de dégradation et des substances relargables

Abstract / scope

This document describes the considerations to include the toxicokinetic evaluation of single chemical which can include its degradant or metabolite known to be released from a medical device. This document provides the principles for designing and performing a toxicokinetic evaluation for medical devices.

Life cycle

Replaces

ISO 10993-16:2017PublishedBiological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesInternational Standard · Published 16 May 2017 · ISO/TC 194