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>UNE EN ISO 10993-16:2018 - Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
sklademVydáno: 2018-05-16
UNE EN ISO 10993-16:2018 - Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)

UNE EN ISO 10993-16:2018

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)

Evaluación biológica de productos sanitarios. Parte 16: Diseño del estudio toxicocinético de productos de degradación y sustancias lixiviables. (ISO 10993-16:2017).

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Označení normy:UNE EN ISO 10993-16:2018
Počet stran:27
Vydáno:2018-05-16
Status:Norma
DESCRIPTION

UNE EN ISO 10993-16:2018

This part of ISO 10993 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.

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