2nd Annual Risk Integration and Quality Management for Medical Devices
July 19 - 20, 2017 - Minneapolis MN US

Attending this marcus evans conference will enable you to take a more holistic and proactive approach to strategic risk management for medical devices. Within each device lifecycle, all potential risks are accounted for, whether they are biological, environmental, software, user error, labeling, or even a risk due to the complexity of use. In order to be effective, companies must employ continuous risk assessments to establish a baseline and categorization of the amount of risk before being able to implement controls to monitor and mitigate that risk. Attendees will develop a strategy to mitigate risk in all phases of the device lifecycle including: planning, policies, procedures, analysis, evaluations, monitoring and controlling of risk.

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