CSA Group Biological evaluation of medical devices - Guidance on the conduct of biological evaluation within a risk management process ISO/TR 15499:2016

Description
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.
Description
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.

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Biological evaluation of medical devices - Guidance on the conduct of biological evaluation within a risk management process - ISO/TR 15499:2016 - CSA Group
Toronto, Ontario, Canada
Biological evaluation of medical devices - Guidance on the conduct of biological evaluation within a risk management process
ISO/TR 15499:2016
Biological evaluation of medical devices - Guidance on the conduct of biological evaluation within a risk management process ISO/TR 15499:2016
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.

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.

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  CSA Group
Product Category Standards and Technical Documents
Product Number ISO/TR 15499:2016
Product Name Biological evaluation of medical devices - Guidance on the conduct of biological evaluation within a risk management process
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