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QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • TF_Legit.Health_Plus
  • 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
  • Procedures
  • Records
  • 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

12 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.)