AAMI/CQT Solutions Design Control Requirements – Integrating The Quality System Regulation and ANSI AAMI ISO 13485 – Ireland – September 30 – October 2

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.

For registration info:  https://my.aami.org/store/events/registration.aspx?event=DCIH093019