Areas of Interest
Conformity Assessment Procedures for CE Certification Device ClassificationTechnical Files for CE CertificationLabeling for CESelf-Certification Procedure (Available ONLY for CLASS I devicesNotified Body selectionProduct Vigilance, within the EUMedical Device Reporting (MDRs), within the EUMore information regarding ‘EU Authorized Representative / Authorized Address’Quotation for services as a 'EU Authorized Representative /Authorized AddressNational RegistrationConsulting
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