AAMI Virtual Event – Design Control Requirements – Integrating the Quality System Regulation – December 3 – 5, 2024
This intensive 3-day, virtual course provides complete coverage of design control requirements for FDA Quality System Regulation, ANSI/AAMI/ISO 13485:2016, and the Medical Device Single Audit Program (MDSAP). With the participation of FDA representatives during the entire course, attendees have the unique opportunity to participate in a shared learning experience. Program Objective Upon completing this course, participants will [...]