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      • 21 CFR 820 QSR
      • ICMED 13485 /ICMED 13485 PLUS
      • GHOST-R
      • ISO 9001:2015
      • ISO 14001:2015
      • ISO 45001:2018
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      • ISO/IEC 17021-1:2015
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      • Legal Metrology Registration
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      • Risk Assessment for Medical Devices – ISO 14971:2019
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      • UDI Implementation Guidance
      • GMDN and EMDN codes research
      • Technical File (TF) Review for MDR 2017/745 & IVDR 2017/746
      • Free Sales Certificate (FSC) for Medical Devices & IVDs
      • Notified Body Selection & Application Support
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      • MDR | Regulation (EU) 2017/745)
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  • Page 31
August 5, 2026

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