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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
    • 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

Records

🗃️ GP-001 Documents and records control

9 items

🗃️ GP-002 Quality planning

14 items

🗃️ GP-003 Audits

6 items

🗃️ GP-004 Vigilance system

2 items

🗃️ GP-005 HR and training

4 items

🗃️ GP-007 Post-market surveillance

1 item

🗃️ GP-009 Sales

1 item

🗃️ GP-010 Suppliers

3 items

🗃️ GP-012 Design, Redesign and Development

3 items

🗃️ GP-018 Infrastructure and facilities

3 items

🗃️ GP-019 Software validation

8 items

🗃️ GP-023 Change control management

3 items

🗃️ GP-050 Data Protection

5 items

🗃️ GP-051 Security violations

3 items

🗃️ GP-052 Data Privacy Impact Assessment (DPIA)

1 item

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GP-101 Information security
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GP-001 Documents and records 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.)