Skip to main content
QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • Legit.Health Plus Version 1.1.0.0
    • Index of Technical Documentation or Product File
    • Summary of Technical Documentation (STED)
    • Description and specifications
    • R-TF-001-007 Declaration of conformity
    • GSPR
    • Artificial Intelligence
    • Clinical
    • Cybersecurity
    • Design and development
    • Design History File
    • IFU and label
    • Post-Market Surveillance
    • Quality control
    • Risk Management
    • Usability and Human Factors Engineering
  • Legit.Health Plus Version 1.1.0.1
  • Licenses and accreditations
  • Applicable Standards and Regulations
  • Grants
  • Public tenders
  • Legit.Health Plus Version 1.1.0.0

Legit.Health Plus Version 1.1.0.0

📄️ Index of Technical Documentation or Product File

For Legit.Health Plus Version 1.1.0.0

📄️ Summary of Technical Documentation (STED)

Manufacturer details

📄️ Description and specifications

Manufacturer details

📄️ R-TF-001-007 Declaration of conformity

This document is a draft version.

🗃️ GSPR

1 item

🗃️ Artificial Intelligence

9 items

🗃️ Clinical

3 items

🗃️ Cybersecurity

8 items

🗃️ Design and development

4 items

🗃️ Design History File

6 items

🗃️ IFU and label

2 items

🗃️ Post-Market Surveillance

4 items

🗃️ Quality control

1 item

🗃️ Risk Management

3 items

🗃️ Usability and Human Factors Engineering

7 items

Previous
Acta de Nombramiento del Responsable de Seguridad ENS
Next
Index of Technical Documentation or Product File
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.)