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AAMI TIR102:2019

U.S. FDA 21 CFR mapping to the applicable regulatory requirement references in ISO 13485:2016 Quality Management Systems
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AAMI TIR102:2019

U.S. FDA 21 CFR mapping to the applicable regulatory requirement references in ISO 13485:2016 Quality Management Systems

PUBLISH DATE 2019
AAMI TIR102:2019
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.
SDO AAMI: Assoc. for the Advancement of Medical Instrumentation
Document Number AAMI TIR102
Publication Date Aug. 30, 2019
Language en - English
Page Count
Revision Level
Supercedes
Committee
Publish Date Document Id Type View
Aug. 30, 2019 AAMI TIR102:2019 Revision