ISO/TR 15499:2016

Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management process

Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management process

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Referenced standards

ISO 10993-11:2006ISO 10993-12:2012ISO 10993-13:2010ISO 10993-14:2001ISO 10993-15:2000ISO 10993-16:2010ISO 10993-17:2002ISO 10993-18:2005ISO 10993-1:2009ISO 10993-7:2008ISO 10993-9:2009ISO 13485:2016ISO 14971:2007ISO/IEC 17025:2005ISO/TS 10993-19:2006
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ISO/TR 15499:2016

Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management process

Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management process

ISO/TR 15499:2016 is applicable to the conduct of biological evaluation of medical devices according to the requirements of ISO 10993-1. It does not add to, or otherwise change, the requirements of ISO 10993-1. This document does not include requirements to be used as the basis of regulatory inspection or certification assessment activities.

This guidance is applicable to all biological evaluation of all types of medical devices including active, non-active, implantable and non-implantable medical devices.

Edition2016
Published Date2016
Published ByInternational Standardization Organisation/Technical Reference
Page Count15