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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
    • 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
      • 09_01_Directive 2013_55_EU_Recognition of Professional Qualifications
      • 09_02_Ley 16_1997 Regulaci贸n de servicios de las Oficinas de Farmacia
      • 09_03_BOE-A-2015 Usos medicamentos y productos sanitarios
      • 09_04_Consenso sobre atenci贸n farmac茅utica
    • 10 Other
    • 11 UK 馃嚞馃嚙 Medical devices
    • 12 EU 馃嚜馃嚭 AI Act
  • External documentation
  • 09 Pharmacy
  • 09_01_Directive 2013_55_EU_Recognition of Professional Qualifications

09_01_Directive 2013_55_EU_Recognition of Professional Qualifications

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09_02_Ley 16_1997 Regulaci贸n de servicios de las Oficinas de Farmacia
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.)