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QMS
  • Welcome to your QMS
  • Quality Manual
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  • Legit.Health Plus Version 1.1.0.0
    • Index
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    • Information provided by the Manufacturer
    • Design and Manufacturing Information
    • GSPR
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          • BI 2024
          • COVIDX EVCDAO 2022
          • DAO Derivación O 2022
          • DAO Derivación PH 2022
          • IDEI 2023
          • MC EVCDAO 2019
          • PH 2024
          • SAN 2024
            • R-TF-015-004 Clinical investigation plan
            • R-TF-015-006 Clinical investigation report
            • R-TF-015-010 Annex E ISO 14155
        • R-TF-015-008 Clinical development plan
    • Design History File
    • Post-Market Surveillance
  • Legit.Health Plus Version 1.1.0.1
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  • SAN 2024

SAN 2024

📄️ R-TF-015-004 Clinical investigation plan

Scope

📄️ R-TF-015-006 Clinical investigation report

Research Title

📄️ R-TF-015-010 Annex E ISO 14155

| Document Title | Purpose | Included | Justification if not provided |

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R-TF-015-010 Annex E ISO 14155
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R-TF-015-004 Clinical investigation plan
All the information contained in this QMS is confidential. The recipient agrees not to transmit or reproduce the information, neither by himself nor by third parties, through whichever means, without obtaining the prior written permission of Legit.Health (AI LABS GROUP S.L.)