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ISO 10993-16:2017 (R2022)
Biological evaluation of medical devices
Part 16: Toxicokinetic study design for degradation products and leachables
Part 16: Toxicokinetic study design for degradation products and leachables
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Summary
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.
Notes
90.92 : Norme internationale à réviser
Technical characteristics
| Publisher | International Organization for Standardization (ISO) |
| Publication Date | 05/16/2017 |
| Confirmation Date | 09/05/2022 |
| Edition | 3 |
| Page Count | 13 |
| EAN | --- |
| ISBN | --- |
| Weight (in grams) | --- |
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16/05/2017
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