EUROPE: Quality System Regulation 21 CFR 820 & ANSI/AAMI/ISO 13485
April
19

EUROPE: Quality System Regulation 21 CFR 820 & ANSI/AAMI/ISO 13485

 April 19 to April 23, 2021 

It is an online event.


This 4.5-day course is the culmination of years of consensus development on the part of a respected group of quality system experts from leading device manufacturers, the FDA, industry consultants, and members of International Organization for Standardization (ISO) standards development teams. Participants will learn how to develop and maintain a quality system program that conforms with the FDA’s Quality System Regulation (21 CFR 820) and ANSI/AAMI/ISO 13485:2016.

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