Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)
医疗器械的生物学评估 - 第16部分:降解产物和可浸出物的毒代动力学研究设计(ISO 10993-16:2010)
发布日期:
2010-02-15
废止日期:
2017-12-06
ISO 10993-16:2010给出了如何设计和执行与医疗器械相关的毒素动力学研究的原理。附录A描述了将毒代动力学研究纳入医疗器械生物学评估的考虑因素
ISO 10993-16:2010 gives principles on how toxicokinetic studies relevant to medical devices should be designed and performed. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.