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The European Database for Medical Devices (EUDAMED)

ClinChoice leverages dedicated teams of in-house regulatory strategists and in-country affiliates who support the preparation, registration, and maintenance of regulatory data in EUDAMED.

  • Complete EUDAMED Support Solutions

    • Complete assessment of supply chain and regulatory activities required to support the submission of data to EUDAMED
    • Inventory of medical devices subject to EUDAMED regulatory requirements for further assessment
    • Assessment and submittal of data for registration of certain European Economic Operators (EO) to obtain Actor Identifier/Single Registration Number (Actor ID/SRN) for each role
    • Identify and support process improvements to support the submission of appropriate data in EUDAMED
    • Assess the overall readiness of the organization to meet EU regulatory reporting requirements