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Event Registration - Design Control Requirements - Integrating The Quality System Regulation and ANSI AAMI ISO 13485

Start Date:
Monday, September 21, 2020
End Date:
Wednesday, September 23, 2020
8:00 AM - 5:00 PM Eastern Daylight Time
  • Benefit from an intensive focus on design control requirements for the FDA’s Quality System Regulation, ANSI/AAMI/ISO 13485:2016, and the Medical Device Single Audit Program (MDSAP)

Registration Fees:

  • AAMI Members: $2340
  • Nonmembers: $2600
  • Government Employees: $935

(All registration fees are to be made payable in U.S. Dollars, payments submitted via check must be drawn on a U.S. Bank)

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