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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
    • 09 Pharmacy
    • 10 Other
      • 10_01_BOE-A-2019-3481 RD Ley precariedad laboral
      • 10_02_Directive 2022_2555_Cybersecurity
    • 11 UK πŸ‡¬πŸ‡§ Medical devices
    • 12 EU πŸ‡ͺπŸ‡Ί AI Act
  • External documentation
  • 10 Other
  • 10_02_Directive 2022_2555_Cybersecurity

10_02_Directive 2022_2555_Cybersecurity

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11 UK πŸ‡¬πŸ‡§ Medical devices
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.)