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BSI - BS EN ISO 10993-16

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

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Organization: BSI
Publication Date: 31 January 2018
Status: active
Page Count: 28
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

BS EN ISO 10993-16
January 31, 2018
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
January 31, 2018
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
January 31, 2018
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
March 31, 2010
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
A description is not available for this item.
July 31, 2009
Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables
This part of ISO 10993 gives principles on how toxicokinetic studies relevant to medical devices should be designed and performed. Annex A describes the considerations for inclusion of toxicokinetic...
November 15, 1997
Biological Evaluation of Medical Devices Part 16: Toxicokinetic Study Design for Degradation Products and Leachables
A description is not available for this item.

References

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