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PubMed · 16259155

Understanding US labelling requirements.

Maria Donawa
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Abstract

Medical device manufacturers should not assume that the information and symbols on labels for the European market are always suitable to meet United States (US) requirements. This article discusses US labelling requirements and how they differ from European requirements.

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DocumentationEquipment and SuppliesEuropeGovernment RegulationGuideline AdherenceGuidelines as TopicProduct LabelingUnited StatesUnited States Food and Drug AdministrationComparative StudyJournal Article

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Maria Donawa. 2005. Understanding US labelling requirements.. https://pubmed.ncbi.nlm.nih.gov/16259155/

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