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General Aspects of Medical Devices
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Event Registration - Risk Management and Human Factors
June 02, 2020
June 03, 2020
[add to calendar]
Training focuses on:
Managing risk across the product life cycle
Identifying use-related hazards and failure modes
Crucial tasks for testing, evaluating failures and addressing use-risk design changes
Post-market complaint investigations
Obtain an understanding of the expectations of the FDA as well as best practices for human factors risk management
Learn how to incorporate risk management activities into their human factors planning
AAMI Members: $1980
Government Employees: $800
AAMI Conference Center
901 North Glebe Road, Suite 300
Arlington, VA 22203
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