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QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • Legit.Health Plus Version 1.1.0.0
  • Legit.Health Plus Version 1.1.0.1
  • Licenses and accreditations
  • External documentation
    • 01 ES πŸ‡ͺπŸ‡Έ regulations
    • 02 US πŸ‡ΊπŸ‡Έ CFR FDA
    • 03 Clinical studies
      • 03_01_ICH-guideline-good-clinical-practice
    • 04 EU πŸ‡ͺπŸ‡Ί Medical devices
    • 05 GP-004 Vigilance system
    • 06 Machine learning
    • 07 Quality regulations
    • 08 MX πŸ‡²πŸ‡½ regulations
    • 09 Pharmacy
    • 10 Other
    • 11 UK πŸ‡¬πŸ‡§ Medical devices
    • 12 EU πŸ‡ͺπŸ‡Ί AI Act
  • External documentation
  • 03 Clinical studies
  • 03_01_ICH-guideline-good-clinical-practice

03_01_ICH-guideline-good-clinical-practice

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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.)