Skip to main content
WHO | World Health Organization

Languages

  • العربية
  • English
  • Français
  • Русский
  • Español
  • Türkçe

Main menu

  • Home
  • Quality Management
  • User Instructions
  • Phase 1
    • Roadmap structure
    • Quality systems essentials structure
      • Facilities & Safety
      • Organization
      • Personnel
      • Equipment
      • Purchasing & Inventory
      • Process Management
      • Information Management
      • Documents and Records
      • Customer Focus
      • Assessment
      • Nonconforming Event Management
      • Continual Improvement
  • Phase 2
    • Roadmap structure
    • Quality systems essentials structure
      • Facilities & Safety
      • Organization
      • Personnel
      • Equipment
      • Purchasing & Inventory
      • Process Management
      • Information Management
      • Documents and Records
      • Customer Focus
      • Assessment
      • Nonconforming Event Management
      • Continual Improvement
  • Phase 3
    • Roadmap structure
    • Quality systems essentials structure
      • Facilities & Safety
      • Organization
      • Personnel
      • Equipment
      • Purchasing & Inventory
      • Process Management
      • Information Management
      • Documents and Records
      • Customer Focus
      • Assessment
      • Nonconforming Event Management
      • Continual Improvement
  • Phase 4
    • Roadmap structure
    • Quality systems essentials structure
      • Facilities & Safety
      • Organization
      • Personnel
      • Equipment
      • Purchasing & Inventory
      • Process Management
      • Information Management
      • Documents and Records
      • Customer Focus
      • Assessment
      • Nonconforming Event Management
      • Continual Improvement
  • Checklists
  • About this tool
    • Acknowledgements
    • Your feedback
    • Download

You are here

Home » ISO15189:2012 - 5.2.3

ISO15189:2012 - 5.2.3

Write an SOP on Information Management

Establish an archive ensuring protection of laboratory information but also enables quick retrieval of information

Arrange and monitor adequate storage space and conditions for samples, documents, records, equipment, consumables, etc.

Store supplies appropriately

Make an inventory list of all hazardous materials and their location within the facility

Separate laboratory areas to prevent cross contamination and optimize the floor plan

Perform a facility and safety assessment

Search this site

Questions on how it works?

Watch the LQSI tutorial

  • © WHO 2015 - 2025

LQSI tool version: 1.0

LQSI tool version: 1.0