AAMI TIR102:2019

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This document provides a mapping of the US FDA 21 CFR requirements to the “regulatory requirements” references in ISO 13485:2016. This mapping is intended to be a tool for US industry to help identify the regulatory requirements from the US medical device regulations to be addressed through an ISO 13485 quality management system.

Product Details

Published:
08/30/2019
ISBN(s):
9781570207242
Number of Pages:
146
File Size:
1 file , 1.1 MB

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