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
Useful links
Organised by
GlobalCompliancePanel
Contact information
Related events
TAC 2025 - 60th Anniversary Conference
14 April 2025 09:00 - 16 April 2025 17:00, Guildford, United Kingdom
九州影院 Teaching in Practice
9 January 2025 09:30-16:00, Oxford, United Kingdom
Advancements in prosthetic/artificial heart valve devices
25 February 2025 17:00-18:30, United Kingdom
Top of the Bench Lancashire Local Section Heat
16 January 2025 10:00-15:30, Preston, United Kingdom
Search
Advertisement
Spotlight
Explore
Membership
