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.
Revises
ISO 10993-16:1997
WITHDRAWN
ISO 10993-16:2010
95.99
Withdrawal of Standard
May 16, 2017
PUBLISHED
ISO 10993-16:2017
Only informative sections of projects are publicly available. To view the full content, you will need to members of the committee. If you are a member, please log in to your account by clicking on the "Log in" button.