ISO 10993-16:2010 PDF
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Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables
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.
| Edition | 2010 |
|---|---|
| Standard Part No | 16 |
| Published Date | 2010 |
| Published By | International Standardization Organisation |
| Page Count | 11 |
