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> Role of Authorized Rep Explained in EU Guideline
Devices & Diagnostics Letter
March 12, 2012
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39 No.
11
Role of Authorized Rep Explained in EU Guideline
The European Commission has published a final guideline aimed at clarifying the relationship between devicemakers and their authorized representatives (AR). It also spells out European Union (EU) member states’ expectations of ARs and their client relationships.
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