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Understanding the Promotion of Medical Devices in the European Union

February 2010

Journal of Medical Device Regulation
Understanding the rules governing the promotion of medical devices in the European Union (EU) can be complex for many reasons. Unlike medicinal products, for which a specific chapter on promotion is dedicated in Directive 2001/83/EC, EU legislation does not contain much in the way of direct rules and guidance that are specific to the promotion and marketing of medical devices.

The team

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