AAMI TIR102 – U.S. FDA 21 CFR mapping to the applicable regulatory requirement references in ISO 13485:2016 Quality Management Systems
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
Note:
This product is unavailable in Russia, Ukraine, Belarus
