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  • Welcome to your QMS
  • Quality Manual
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  • Legit.Health Plus Version 1.1.0.0
  • Legit.Health Plus Version 1.1.0.1
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    • 01 ES πŸ‡ͺπŸ‡Έ regulations
    • 02 US πŸ‡ΊπŸ‡Έ CFR FDA
    • 03 Clinical studies
    • 04 EU πŸ‡ͺπŸ‡Ί Medical devices
      • 04_01_2007_MDD 93_42_EEC
      • 04_02_2017_745-MDR_20200424_EN
      • 04_03_2017_2185 MD coding
      • 04_04_2023_607_MDR & IVDR transition approval
      • 04_05_2012_207_en_Electronic IFU
      • 04_06_2021_2226_en_Electronic IFU
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    • 05 GP-004 Vigilance system
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    • 07 Quality regulations
    • 08 MX πŸ‡²πŸ‡½ regulations
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    • 11 UK πŸ‡¬πŸ‡§ Medical devices
    • 12 EU πŸ‡ͺπŸ‡Ί AI Act
  • External documentation
  • 04 EU πŸ‡ͺπŸ‡Ί Medical devices
  • 04_02_2017_745-MDR_20200424_EN

04_02_2017_745-MDR_20200424_EN

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