AAMI Virtual Course – Integrating Risk Management into the Product Life Cycle – May 6-8, 2025
This comprehensive 3-day course for medical device manufacturers presents risk management concepts used throughout the quality system that can help your organization meet FDA, ANSI/AAMI/ISO 14971:2019 and ANSI/AAMI/ISO 13485:2016 requirements for risk management. This course covers the use of risk management principles throughout the life cycle of the product, from design to manufacturing through post-production [...]