Risk Management in Medical Devices Industry - US Seminar 2012 at Boston

12 - 13 April 2012, Boston, United States

Introduction

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.