*Virtual Only* – The Quality System Regulation 21 CFR 280 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements – April 27-May 1, 2020 – 8 am – 12 noon ET

• 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
• Content 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 ISO standards development teams

For more details:  https://my.aami.org/store/events/registration.aspx?event=QS0420