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 馃嚜馃嚫 regulations
      • 01_01 Instrucciones de obtenci贸n de licencias de instalaciones
      • 01_02_CERTPS Manual de empresas
      • 01_03_CNCps Gu铆a para la documentaci贸n 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 cl铆nicos
      • 01_08_2021 C贸digo de buenas pr谩cticas de la industria farmac茅utica
    • 02 US 馃嚭馃嚫 CFR FDA
    • 03_Clinical studies
    • 04 EU 馃嚜馃嚭 Medical devices
    • 05_GP-004 Vigilance system
    • 06_Machine learning
    • 07 Quality regulations
    • 08 MX 馃嚥馃嚱 regulations
    • 09 Pharmacy
    • 10 Other
    • 11 UK 馃嚞馃嚙 Medical devices
    • 12 EU 馃嚜馃嚭 AI Act
  • Procedures
  • Records
  • External documentation
  • 01 ES 馃嚜馃嚫 regulations
  • 01_04_BOE-RD 7416_2023 productos sanitarios

01_04_BOE-RD 7416_2023 productos sanitarios

Previous
01_03_CNCps Gu铆a para la documentaci贸n tecnica
Next
01_05_BOE-RD publicidad productos sanitarios
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.)