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QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • TF_Legit.Health_Plus
    • Legit.Health Plus TF index
    • Legit.Health Plus STED
    • Legit.Health Plus description and specifications
    • R-TF-001-007 Declaration of conformity
    • GSPR
    • Clinical
    • Design and development
    • Design History File (DHF)
      • Version 1.1.0.0
        • Requirements
        • Test plans
        • Test runs
        • Review meetings
          • Design (Phase 1)
          • Design (Phase 2)
          • Software development
          • Software verification
          • Software validation
        • 🥣 SOUPs
    • IFU and label
    • Post-Market Surveillance
    • Quality control
    • Risk Management
  • Licenses and accreditations
  • External documentation
  • TF_Legit.Health_Plus
  • Design History File (DHF)
  • Version 1.1.0.0
  • Review meetings
  • Design (Phase 2)

Design (Phase 2)

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Design (Phase 1)
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Software development
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.)