Guidance

WHO manual for organizing a national external quality assessment programme for health laboratories and other testing sites

Results of clinical testing obtained from laboratories or testing sites at or near the point of care must be as accurate as possible as they have a direct impact on care and treatment, prevention, and control of diseases. Testing consists of pre-examination, examination, and post-examination processes, which require strict implementation of a quality management system.

Participation in an “external quality assessment” (EQA) programme allows for a “peer-review” process towards solving technical and methodological problems to improve the quality of service for each individual testing site as well as to achieve comparability of results among different testing services.

This manual describes some of the strategic, managerial, financial, technical and scientific aspects to be considered in establishing a national EQA programme for clinical laboratories and other testing services at all health care levels.

Languages

  • English

Publication year

2016

Publisher

WHO

Type

Guidance

Categories

  • Programme management

Organisations

  • World Health Organisation (WHO)

Tags

  • Disease surveillance

Topic references

EPI-CORE-VPD-SURVEILLANCE

TitleAuthorYearTypeLanguage
Global framework for immunization monitoring and surveillanceCenters for Disease Control and Prevention (CDC), World Health Organization (WHO)2007GuidanceFrench
Global Strategy on Comprehensive Vaccine-Preventable Disease SurveillanceWorld Health Organization (WHO)2020GuidanceEnglish
Laboratory networkWorld Health Organization (WHO)1960RepositoryFrench
Vaccine Preventable Diseases Surveillance StandardsWorld Health Organization (WHO)2018GuidanceRussian
WHO manual for organizing a national external quality assessment programme for health laboratories and other testing sitesWorld Health Organization (WHO)2016GuidanceEnglish