Superseded Standard
Historical

DIN EN ISO 10993-16:2009-08

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:1997); German version EN ISO 10993-16:2009.

Summary

The document 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.

Notes

DIN EN ISO 10993-16 (1997-11) remains valid alongside this standard until 2010-03-21.

Technical characteristics

Publisher Deutsche Institut für Normung e.V. (DIN)
Publication Date 08/01/2009
Page Count 21
EAN ---
ISBN ---
Weight (in grams) ---
No products.

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