Skip to main content
QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • TF_Legit.Health_Plus
  • Licenses and accreditations
  • External documentation
    • 01 ES 🇪🇸 regulations
    • 02 US 🇺🇸 CFR FDA
    • 03_Clinical studies
    • 04 EU 🇪🇺 Medical devices
    • 05_GP-004 Vigilance system
    • 06_Machine learning
      • 06_01_GMLP_Guiding_Principles
      • 06_02_US-FDA-Artificial-Intelligence-and-Machine-Learning-Discussion-Paper
    • 07 Quality regulations
    • 08 MX 🇲🇽 regulations
    • 09 Pharmacy
    • 10 Other
    • 11 UK 🇬🇧 Medical devices
    • 12 EU 🇪🇺 AI Act
  • Procedures
  • Records
  • External documentation
  • 06_Machine learning

06_Machine learning

📄️ 06_01_GMLP_Guiding_Principles

📄️ 06_02_US-FDA-Artificial-Intelligence-and-Machine-Learning-Discussion-Paper

Previous
05_07_T-004_FSCA_Meddev_2-12_1_Rev8
Next
06_01_GMLP_Guiding_Principles
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.)