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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
    • 09 Pharmacy
    • 10 Other
    • 11 UK 🇬🇧 Medical devices
    • 12 EU 🇪🇺 AI Act
  • External documentation

External documentation

🗃️ 01 ES 🇪🇸 regulations

8 items

🗃️ 02 US 🇺🇸 CFR FDA

13 items

🗃️ 03 Clinical studies

1 item

🗃️ 04 EU 🇪🇺 Medical devices

7 items

🗃️ 05 GP-004 Vigilance system

7 items

🗃️ 06 Machine learning

2 items

🗃️ 07 Quality regulations

13 items

🗃️ 08 MX 🇲🇽 regulations

4 items

🗃️ 09 Pharmacy

4 items

🗃️ 10 Other

2 items

🗃️ 11 UK 🇬🇧 Medical devices

1 item

🗃️ 12 EU 🇪🇺 AI Act

1 item

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01 ES 🇪🇸 regulations
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.)