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    • GP-001 Documents and records control
    • GP-002 Quality planning
      • Deprecated
      • R-002-001 Quality objectives list_2024_001
      • R-002-001 Quality objectives list_2025
      • R-002-002 Quality objectives_2024_001
      • R-002-002 Quality objectives_2024_002
      • R-002-002 Quality objectives_2024_003
      • R-002-002 Quality objectives_2024_004
      • R-002-002 Quality objectives_2024_005
      • R-002-002 Quality objectives_2025_001
      • R-002-002 Quality objectives_2025_002
      • R-002-002 Quality objectives_2025_003
      • R-002-002 Quality objectives_2025_004
      • R-002-002 Quality objectives_2025_005
      • R-002-003 Quality indicators_2024
      • R-002-004 Annual management review report
      • R-002-005 Quality Calendar_2025
      • R-002-006 SWOT and CAME analysis
      • R-002-007
      • R-002-008 Quality and regulatory roadmap
      • R-002-009 Regulatory requirements review report
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    • GP-007 Post-market surveillance
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    • GP-018 Infrastructure and facilities
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    • GP-200 Remote Data Acquisition in Clinical Investigations
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  • GP-002 Quality planning
  • R-002-001 Quality objectives list_2024_001

R-002-001 Quality objectives list_2024_001

Objectives list​

NumberBrief descriptionEstablishment dateStatus
01Certify with a notified body the new Class IIa medical device2024-02-13Extended
02Certification of the AI LABS GROUP's QMS under EN-ISO 13485 by a Notified Body2024-02-13Extended
03Register medical device in Mexico, Brazil and USA2024-02-13In progress
04Increase in turnover by 2.5X2024-02-13In progress
05Product meets customer expectations2024-02-13In progress

Record signature meaning

  • Author: JD-004
  • Review and approval: JD-001
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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.)