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ISO 10993-16:2010

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ISO 10993-16:2010 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

standard by International Organization for Standardization, 02/01/2010

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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.

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Published: 02/01/2010File Size: 1 file , 210 KB Same As: BS EN ISO 10993-16:2010, AAMI/ISO 10993-16:2010/(R)2014, BS EN ISO 10993-16:2010