Overview: The course will introduce the main elements of risk management and the application of risk management principles and requirements to the medical device development cycle. Risk management has become the method of choice to ensure an effective and safety oriented device development. International consensus, reflected in globally applicable standard requirements, has led to risk management as a mandatory component of almost any activity in the medical device industry.
Risk Management in Medical Devices Industry - US Seminar 2012 at Boston
12 - 13 April 2012, Boston, United States
Introduction
Venue
Boston Marriott Long Wharf
Boston Marriott Long Wharf, Boston, United States
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Organised by
GlobalCompliancePanel
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