Design Control Requirements – Integrating the Quality System Regulation – September 10 – 12, 2024
Overview This intensive 3 – day 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. Objectives Upon completing this [...]