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 » ISO15189:2007 - 5.2.1

ISO15189:2007 - 5.2.1

Create a primary sample collection facility separate from the laboratory

When the laboratory works with pathogens requiring a biosafety level (BSL) III facility: create a negative pressure laboratory

Ensure uninterrupted supply of electricity

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

Perform a facility and safety assessment

Determine which biosafety level the facilities need to comply with

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