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Medical Device

Medical DeviceHealth authorities are increasingly raising the demands on documentation of medical devices.

The IWA Consulting Team can assist your organization in setting up appropriate quality systems,  classification evaluations, and Conformity Assessment Procedures to select the appropriate route for CE marking.

The IWA Consulting Team has experience in preparing dossiers including those for Notified Bodies and other relevant parties.


For more information on our services for medtech, please contact Medical Device RA & QA Team.