This course provides an overview of international medical device regulations. Beginning with a discussion of the similarity of global requirements, including both voluntary and mandatory standards and directives, and progressing to in-depth analyses of market specific requirements.
2-day In-person Seminar on Global Medical Device Regulation: US, EU and Canada at Chicago IL
4 - 5 September 2014, Chicago, United States
Introduction
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WILL BE ANNOUNCED SOON
WILL BE ANNOUNCED SOON, Chicago, Chicago, United States
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GlobalCompliancePanel
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