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  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
    • GP-001 Documents and records control
      • Deprecated
        • R-001-001 Control of documents and records
        • R-001-001 Control of documents and records_2023_001
        • R-001-001 Control of documents and records 2023_002
        • R-001-001 Control of documents 2023_003
        • R-001-001 Control of documents 2023_003
        • R-001-002 2020_001 Manufacturer declaration of conformity
        • R-001-002 2021_001 Manufacturer declaration of conformity
        • R-001-002 2021_002 Manufacturer declaration of conformity
        • R-001-002 2021_003 Manufacturer declaration of conformity
        • R-001-002 2021_004 Manufacturer declaration of conformity
        • R-001-002 2023_001 Manufacturer declaration of conformity
        • R-001-002 Manufacturer declaration of conformity_2023_002
        • R-001-003 Backup copies control
        • R-001-004 Backup integrity verification
        • R-001-005 List of external documents_2023_001
        • R-001-005 List of external documents_2023_002
        • R-001-005 List of external documents_2023_003
        • R-001-005 List of external documents_2023_004
      • R-001-001 Control of documents
      • R-001-002 Manufacturer declaration of conformity for Brazil
      • R-001-002 Manufacturer declaration of conformity
      • R-001-005 List of applicable standards and regulations
      • R-001-008 Legit.Health Plus label for Brazil
      • R-001-009 Training on procedures of the QMS
      • R-001-009 Training on procedures of the QMS
      • R-001-009 Training on procedures of the QMS
      • R-001-009 Training on procedures of the QMS
      • R-001-009 Training on procedures of the QMS
    • 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
    • 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
  • Licenses and accreditations
  • Applicable Standards and Regulations
  • Grants
  • Pricing
  • Public tenders
  • Records
  • GP-001 Documents and records control
  • Deprecated
  • R-001-003 Backup copies control

R-001-003 Backup copies control

  • Governed by GP-001 Document and Registry Control
  • Comes from template T-001-003
Written byReviewed byApproved by

E-Signature (Appfire integration):

Signature logo

Alfonso Medela

C89F81C7B363885F7F9D8A5882E45A0E

Signer name: Alfonso Medela

Signing time: Fri, 06 Jan 2023 17:41:07 GMT

Reason: Creation of document

E-Signature (Appfire integration):

Signature logo

Taig Mac Carthy

610FD2500F1DCDDC700FF0ED05D48E26

Signer name: Taig Mac Carthy

Signing time: Mon, 09 Jan 2023 14:41:07 GMT

Reason: Reviewed

E-Signature (Appfire integration):

Signature logo

Andy Aguilar

F3EFACAE01947494C8DA3B103B6D05DE

Signer name: Andy Aguilar

Signing time: Mon, 09 Jan 2023 17:45:07 GMT

Reason: Approving document

JD-005 Technical ManagerJD-004 Quality ManagerJD-001 General Manager

Backup copies control​

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R-001-004 Backup integrity verification
  • Backup copies control
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.)