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QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
    • GP-001 Documents and records control
    • GP-002 Quality planning
    • GP-003 Audits
    • GP-004 Vigilance system
    • GP-005 HR and training
    • GP-007 Post-market surveillance
    • GP-009 Sales
    • GP-010 Suppliers
      • 🔍 Evidence
      • Deprecated
        • R-010-001 Suppliers evaluation 2023_001
        • R-010-001 Suppliers evaluation 2023_002
        • R-010-001 Suppliers evaluation
        • R-010-001 Suppliers evaluation 20_001
        • R-010-001 Suppliers evaluation 21_001
        • R-010-001 Suppliers evaluation 21_001
        • R-010-001 Suppliers evaluation 22_001
        • S-AMA-QMS Certification
      • R-010-001 Suppliers evaluation
    • GP-012 Design, Redesign and Development
    • GP-018 Infrastructure and facilities
    • GP-019 Software validation
    • GP-023 Change control management
    • GP-050 Data Protection
    • GP-051 Security violations
    • GP-052 Data Privacy Impact Assessment (DPIA)
  • TF_Legit.Health_Plus
  • Licenses and accreditations
  • External documentation
  • Procedures
  • Records
  • Records
  • GP-010 Suppliers
  • Deprecated
  • S-AMA-QMS Certification

S-AMA-QMS Certification

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R-010-001 Suppliers evaluation 22_001
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R-010-001 Suppliers evaluation
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.)