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 🇪🇸 regulations
    • 02 US 🇺🇸 CFR FDA
    • 03_Clinical studies
    • 04 EU 🇪🇺 Medical devices
    • 05_GP-004 Vigilance system
      • 05_01_T-004_TREND REPORT_Meddev_2-12_1_Rev8
      • 05_02_T-004_PSR_Meddev_2-12_1_Rev8
      • 05_03_T-004_NCA REPORT_Meddev_2-12_1_Rev8
      • 05_04_T-004_MIR_Meddev_2-12_1_Rev8
      • 05_05_MIR_form_v7.2.1b
      • 05_06_T-004_FSN_Meddev_2-12_1_Rev8
      • 05_07_T-004_FSCA_Meddev_2-12_1_Rev8
    • 06_Machine learning
    • 07 Quality regulations
    • 08 MX 🇲🇽 regulations
    • 09 Pharmacy
    • 10 Other
    • 11 UK 🇬🇧 Medical devices
    • 12 EU 🇪🇺 AI Act
  • External documentation
  • 05_GP-004 Vigilance system
  • 05_04_T-004_MIR_Meddev_2-12_1_Rev8

05_04_T-004_MIR_Meddev_2-12_1_Rev8

Previous
05_03_T-004_NCA REPORT_Meddev_2-12_1_Rev8
Next
05_05_MIR_form_v7.2.1b
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.)