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Event Registration - The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements
Monday, September 07, 2020
Friday, September 11, 2020
8:00 AM - 12:00 PM Eastern Daylight Time
  • Learn how to develop and maintain a quality system program that conforms with the FDA’s Quality System Regulation (21 CFR 820) and ANSI/AAMI/ISO 13485:2016
  • Content is the culmination of years of consensus development on the part of a respected group of quality system experts from leading device manufacturers, the FDA, industry consultants and members of ISO standards development teams

Registration Fees:

  • AAMI Members: $3060
  • Nonmembers: $3400
  • Government Employees: $1225
(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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