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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
      • 2024-2025
        • 🔍 Evidence
          • S-AMA
          • S-APO
          • S-ATL
          • S-FAC
          • S-GOO
          • S-HUB
          • S-IDI
          • S-MIC
          • S-SLA
          • S-STR
          • S-THA
        • R-010-001 Suppliers evaluation
        • R-010-002 Approved suppliers list 2025
      • 2026-2027
      • 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)
    • GP-200 Remote Data Acquisition in Clinical Investigations
    • GP-011 Provision of service
    • GP-110 Esquema Nacional de Seguridad
  • Legit.Health Plus Version 1.1.0.0
  • Legit.Health Plus Version 1.1.0.1
  • Legit.Health Utilities
  • Licenses and accreditations
  • Applicable Standards and Regulations
  • Pricing
  • Public tenders
  • Records
  • GP-010 Suppliers
  • 2024-2025
  • 🔍 Evidence
  • S-AMA

S-AMA

S-AMA-ISMS Certification​

S-AMA-QMS Certification​

S-AMA-ENS Alta Certification B0185​

S-AMA-ENS Alta Certification B0218​

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S-APO
  • S-AMA-ISMS Certification
  • S-AMA-QMS Certification
  • S-AMA-ENS Alta Certification B0185
  • S-AMA-ENS Alta Certification B0218
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.)