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 implement and maintain a risk-based quality management system that complies with FDA’s amended 21 CFR 820 and the Quality Management System Regulation (QMSR).
For more info: https://aami.my.site.com/s/lt-event?id=a1YUW00000FHh7y