2nd Annual Risk Integration and Quality Management for Medical Devices
Event Jul 19 - Jul 20, 2017
Location: Minneapolis, MN, USA
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.
This conference will bring together quality, regulatory affairs, and compliance professionals to benchmark current risk management strategies against other peer organizations, interpret new FDA and European guidance’s, as well as analyze the ISO 13485 and 14971 standards.”
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