The course is based on 20+ years of experience in the medical device industry and emphasizes practical implementation issues and not just theoretical background. If your company is developing devices for international markets this seminar will give you the information needed to design and document a globally acceptable design lifecycle.
2-day In-person seminar on Implementing Risk Management Principles and Activities within a Quality Management System at Sydney, Australia
24 - 25 February 2014, Sydney, Australia
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Sydney, Australia
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GlobalCompliancePanel
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