AAMI - TIR15499
Biological evaluation of medical devices–Guidance on the conduct of biological evaluation within a risk management process
inactive
| Organization: | AAMI |
| Publication Date: | 1 January 2012 |
| Status: | inactive |
| Page Count: | 30 |
scope:
This Technical Report 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 Technical Report 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.
Document History
January 1, 2017
Biological evaluation of medical devices-Guidance on the conduct of biological evaluation within a risk management process
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...
TIR15499
January 1, 2012
Biological evaluation of medical devices–Guidance on the conduct of biological evaluation within a risk management process
This Technical Report 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...