Skip to main content
QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • Legit.Health Plus Version 1.1.0.0
    • Index
    • Overview and Device Description
    • Information provided by the Manufacturer
    • Design and Manufacturing Information
      • Product Requirement Specification (PRS)
      • Software Requirement Specification (SRS)
      • R-TF-012-019 SOUPs
      • R-TF-012-023 Software Development Plan
      • R-TF-012-030 Software Configuration Management Plan
      • Review meetings
        • Design (Phase 1) Review
        • Design (Phase 2) Review
        • Software development review
        • Software verification review
        • Software validation review
      • R-TF-012-033 Software Tests Plan
      • R-TF-012-037 Labeling and IFU Requirements
      • deprecated
    • GSPR
    • Benefit-Risk Analysis and Risk Management
    • Product Verification and Validation
    • Post-Market Surveillance
  • Legit.Health Plus Version 1.1.0.1
  • Licenses and accreditations
  • Applicable Standards and Regulations
  • Grants
  • Pricing
  • Public tenders
  • Legit.Health Plus Version 1.1.0.0
  • Design and Manufacturing Information
  • Review meetings
  • Design (Phase 2) Review

Design (Phase 2) Review

Previous
Design (Phase 1) Review
Next
Software development review
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.)