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
    • Clinical
      • Evaluation
        • R-TF-015-001 Clinical Evaluation Plan
        • R-TF-015-002 Preclinical and clinical evaluation record_2023_001
        • R-TF-015-003 Clinical Evaluation Report
        • R-TF-015-007 Delaration of interest Alberto Sabater
        • R-TF-015-007 Delaration of interest Alfonso Medela
        • R-TF-015-007 Delaration of interest Constanza Balboni
        • R-TF-015-007 Delaration of interest María Belén Hirigoity
        • R-TF-015-007 Delaration of interest María Diez
        • R-TF-015-007 Delaration of interest Taig Mac Carthy
      • Investigation
      • R-TF-015-008 Clinical development plan
    • 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
  • External documentation
  • Legit.Health Plus Version 1.1.0.0
  • Clinical
  • Evaluation
  • R-TF-015-007 Delaration of interest María Belén Hirigoity

R-TF-015-007 Delaration of interest María Belén Hirigoity

Your browser does not support viewing PDFs.Download PDF
Previous
R-TF-015-007 Delaration of interest Constanza Balboni
Next
R-TF-015-007 Delaration of interest María Diez
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.)