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KAREV
  • HomePage
  • Corporate
    • About Us
    • Logos
    • Management’s Commitment
    • Quality Policy
    • Accreditations
  • Our Services
    • System Certification
      • EN ISO 13485:2016
    • Trainings
      • Standart Trainings
        • EN ISO 14971:2019 Product Risk Management
        • ISO 13485:2016 Medical Device Quality Management System
      • Regulational Trainings
        • MDR:2017/745
      • Special Process Trainings
        • Validation Trainings
  • Documents
  • Career
  • Announcements
  • Contact
  • English
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Regulational Trainings

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Training

Standard Trainings
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CE Certification

Medical Devices Regulation (EU) 2017/745
In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746

System Certification

EN ISO 13485:2016
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