Skip to main content
QMSQMS
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 🇪🇸 regulations
    • 02 US 🇺🇸 CFR FDA
    • 03 Clinical studies
    • 04 EU 🇪🇺 Medical devices
    • 05 GP-004 Vigilance system
    • 06 Machine learning
    • 07 Quality regulations
    • 08 MX 🇲🇽 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 🇬🇧 Medical devices
    • 12 EU 🇪🇺 AI Act
  • External documentation
  • 08 MX 🇲🇽 regulations

08 MX 🇲🇽 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

Previous
ISO 62304_2007
Next
08_01_Ley Reforma Salud MX
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.)