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      • ISO 13485:2016 & EN ISO 13485:2016 + A11:2021
      • Medical Device Single Audit Program (MDSAP)
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      • GHOST-R
      • ISO 9001:2015
      • ISO 14001:2015
      • ISO 45001:2018
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      • ISO/IEC 17021-1:2015
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      • ISO/IEC 17024:2012
      • CDSCO Notified Body Approval
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      • Ethics Committee Approval – CDSCO/ICMR for Medical Devices
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      • IP ACT- TRADE MARK / PATENT
      • CPCP-PWM/ EWM
      • Legal Metrology Registration
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      • USA-USFDA
      • SFDA-MENA
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      • Risk Assessment for Medical Devices – ISO 14971:2019
      • CER, PMS, PMCF, PSUR, SSCP
      • EUDAMED Registration Services
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      • 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 33
August 5, 2026

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Friday, 17 July 2026 by orion45641

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