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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.100 Laboratory medicine>11.100.20 Biological evaluation of medical devices>PD ISO/TR 15499:2016 Biological evaluation of medical devices. Guidance on the conduct of biological evaluation within a risk management process
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immediate downloadReleased: 2017-01-31
PD ISO/TR 15499:2016 Biological evaluation of medical devices. Guidance on the conduct of biological evaluation within a risk management process

PD ISO/TR 15499:2016

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

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Standard number:PD ISO/TR 15499:2016
Pages:26
Released:2017-01-31
ISBN:978 0 580 95983 7
Status:Standard
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PD ISO/TR 15499:2016


This standard PD ISO/TR 15499:2016 Biological evaluation of medical devices. Guidance on the conduct of biological evaluation within a risk management process is classified in these ICS categories:
  • 11.100.20 Biological evaluation of medical devices

This document 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.