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QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
    • GP-001 Control of documents
    • GP-002 Quality planning
    • GP-003 Audits
    • GP-004 Vigilance system
    • GP-005 Human Resources and Training
    • GP-006 Non-conformity, Corrective and Preventive actions
    • GP-007 Post-market surveillance
    • GP-008 Product requirements
    • GP-009 Sales
    • GP-010 Purchases and suppliers evaluation
    • GP-011 Provision of service
    • GP-012 Design, Redesign and Development
    • GP-013 Risk management
    • GP-014 Feedback and complaints
    • GP-015 Clinical evaluation
    • GP-016 Traceability and identification
    • GP-017 Technical assistance service
    • GP-018 Infrastructure and facilities
    • GP-019 Software validation plan
    • GP-020 QMS Data analysis
    • GP-021 Communications
    • GP-022 Document translation
    • GP-023 Change control management
    • GP-024 Cybersecurity
    • GP-025 Corporate Governance
    • GP-026 Product requirements for US market
    • GP-027 Product requirements for UK market
    • GP-028 Product requirements for the Brazilian market
    • GP-050 Data Protection
    • GP-051 Security violations
    • GP-052 Data Privacy Impact Assessment (DPIA)
    • GP-100 Business Continuity (BCP) and Disaster Recovery plans (DRP)
    • GP-101 Information security
    • GP-200 Remote Data Acquisition in Clinical Investigations
  • Records
  • TF_Legit.Health_Plus
  • Licenses and accreditations
  • External documentation
  • Procedures

Procedures

🗃️ GP-001 Control of documents

4 items

🗃️ GP-002 Quality planning

1 item

🗃️ GP-003 Audits

1 item

🗃️ GP-004 Vigilance system

2 items

🗃️ GP-005 Human Resources and Training

2 items

📄️ GP-006 Non-conformity, Corrective and Preventive actions

Procedure flowchart

🗃️ GP-007 Post-market surveillance

1 item

🗃️ GP-008 Product requirements

1 item

🗃️ GP-009 Sales

3 items

🗃️ GP-010 Purchases and suppliers evaluation

1 item

🗃️ GP-011 Provision of service

1 item

🗃️ GP-012 Design, Redesign and Development

3 items

🗃️ GP-013 Risk management

1 item

🗃️ GP-014 Feedback and complaints

1 item

🗃️ GP-015 Clinical evaluation

1 item

📄️ GP-016 Traceability and identification

Purpose

📄️ GP-017 Technical assistance service

Purpose

🗃️ GP-018 Infrastructure and facilities

2 items

🗃️ GP-019 Software validation plan

1 item

🗃️ GP-020 QMS Data analysis

1 item

📄️ GP-021 Communications

Purpose

📄️ GP-022 Document translation

Procedure flowchart

🗃️ GP-023 Change control management

1 item

📄️ GP-024 Cybersecurity

Procedure flowchart

🗃️ GP-025 Corporate Governance

1 item

🗃️ GP-026 Product requirements for US market

1 item

📄️ GP-027 Product requirements for UK market

Purpose

📄️ GP-028 Product requirements for the Brazilian market

Purpose

🗃️ GP-050 Data Protection

2 items

🗃️ GP-051 Security violations

1 item

🗃️ GP-052 Data Privacy Impact Assessment (DPIA)

1 item

📄️ GP-100 Business Continuity (BCP) and Disaster Recovery plans (DRP)

Purpose

📄️ GP-101 Information security

Purpose

🗃️ GP-200 Remote Data Acquisition in Clinical Investigations

1 item

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GP-001 Control of documents
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.)