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QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • TF_Legit.Health_Plus
  • Licenses and accreditations
  • External documentation
    • 01 ES 🇪🇸 regulations
      • 01_01 Instrucciones de obtención de licencias de instalaciones
      • 01_02_CERTPS Manual de empresas
      • 01_03_CNCps Guía para la documentación tecnica
      • 01_04_BOE-RD 7416_2023 productos sanitarios
      • 01_05_BOE-RD publicidad productos sanitarios
      • 01_06_BOE-RD 1591_2009 productos sanitarios
      • 01_07_BOE 1090_2015 Medicamentos y ensayos clínicos
      • 01_08_2021 Código de buenas prácticas de la industria farmacéutica
    • 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
    • 09 Pharmacy
    • 10 Other
    • 11 UK 🇬🇧 Medical devices
    • 12 EU 🇪🇺 AI Act
  • Procedures
  • Records
  • External documentation
  • 01 ES 🇪🇸 regulations
  • 01_06_BOE-RD 1591_2009 productos sanitarios

01_06_BOE-RD 1591_2009 productos sanitarios

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01_07_BOE 1090_2015 Medicamentos y ensayos clínicos
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.)