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Event Registration - The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements

Start Date:
Monday, June 22, 2020
End Date:
Friday, June 26, 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

An optional exam is available online for two weeks following the end of the program.

Registration Fees:

  • AAMI Members: $3060
  • Nonmembers: $3400
  • Government Employees: $1225
  • Event Location
    • Address:
      AAMI Center for Excellence (ACE), 901 North Glebe
      901 North Glebe Road Suite 300
      Arlington, VA 22203

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