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Norm
ISO 10993-16:2017
Issue date: 2017 05 16
Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables
ISO 10993-16:2017 provides principles on designing and performing toxicokinetic studies relevant to medical devices. Annex A describes the considerations for inclusion of...
Valid
Publisher:
International Organization for Standardization
Format:
Digital | 13 Pages
Language:
English
ICS
ISO 10993-16:2017 provides principles on designing and performing toxicokinetic studies relevant to medical devices. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.
ISO 10993-16:2017
2017 05 16
Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation produ...
Norm
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ISO 10993-16:2010
2010 02 09
Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation produ...
Norm
ISO 10993-16:1997
1997 08 28
Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation produ...
Norm
