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European Union Directives

Develop safe and effective medical devices for the European Union

European Union Directives, covering medical devices, are standards that govern product efficacy and safety. Devices must meet or exceed these regulations for use throughout the EU. Adhering to these standards enables you to:

  • Achieve CE Mark status
  • Provide high levels of safety
  • Assure product reliability

Purchase Options

Full Online Standards SolutionIndividual Standards
Multiple standardsMinimal standards
Frequent purchases ($3000+/year)Infrequent purchases
Standards access or budget management, organization-wideLess than 5 employees use standards
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