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 πŸ‡ͺπŸ‡Έ regulations
    • 02 US πŸ‡ΊπŸ‡Έ CFR FDA
    • 03_Clinical studies
    • 04 EU πŸ‡ͺπŸ‡Ί Medical devices
    • 05_GP-004 Vigilance system
    • 06_Machine learning
    • 07 Quality regulations
    • 08 MX πŸ‡²πŸ‡½ regulations
      • 08_01_Ley Reforma Salud MX
      • 08_02_2011_12_31_Listado insumos no MD_DOF
      • 08_03_2014_12_22_Listado insumos no MD_DOF
      • 08_04_Reglamento de Insumos para la salud
    • 09 Pharmacy
    • 10 Other
    • 11 UK πŸ‡¬πŸ‡§ Medical devices
    • 12 EU πŸ‡ͺπŸ‡Ί AI Act
  • External documentation
  • 08 MX πŸ‡²πŸ‡½ regulations
  • 08_01_Ley Reforma Salud MX

08_01_Ley Reforma Salud MX

Previous
08 MX πŸ‡²πŸ‡½ regulations
Next
08_02_2011_12_31_Listado insumos no MD_DOF
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.)