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Impact of ISO/IEC 17025 laboratory accreditation in sub-Saharan Africa: a case study
Mercy A Okezue1,2, Mojisola C Adeyeye3, Steve J Byrn4
1School of Agricultural & Biological Engineering, Biotechnology Innovation & Regulatory Science, Purdue University, West Lafayette, USA. mokezue@purdue.edu.
Background:
The number and severity of nonconformities generated during an audit of a medicine testing laboratory indicates its level of quality compliance. Quality standards are established and maintained to ensure the reliability of laboratory test reports. The National Medicines Regulatory Authority (NMRA) Quality Control laboratories assess the quality of medicines used by the populace as part of their regulatory function. Although countries desire to have reliable medicine testing facilities, accrediting a national laboratory to international standards poses financial and technical challenges for many low-income countries. Sharing the benefits of laboratory accreditation could help more countries within sub-Saharan Africa overcome existing challenges to achieve accreditation and robust quality systems. This study investigated the impact of ISO/IEC 17025 accreditation on the performance of an NMRA Quality Control laboratory to provide evidence of improved quality compliance within a low-resource setting.
Methods:
Pre- and post- accreditation audits of nonconformities for management and technical requirements of the ISO/IEC17025:2005 standards were evaluated from a Quality Control laboratory in the National Agency for Food and Drug Administration and Control (NAFDAC), located in Nigeria, West Africa. The following research questions were addressed: "does accreditation impact the adherence to quality standards?" and "does accreditation decrease the severity of nonconformities in Quality Control laboratory audits?"
Results:
Statistical analysis of the pre- to post- accreditation audits from the years 2013 through 2017 revealed a significant decrease in the total number of nonconformities (χ2 = 74, p-value = 9.99e-05, r = 0.67). Further examination of audits from the years 2013 through 2018 audits also revealed a reduction in the number of nonconformities (χ2 = 53, p-value = 9.99e-05, r = 0.62). A reduction in the number of major observations and a decrease in the severity of nonconformities was also observed.
Conclusions:
A higher level of quality compliance was exhibited for the laboratory during the post-accreditation years. Overall, ISO/IEC 17025 accreditation of the NMRA Quality Control laboratory resulted in improved reliability of test reports and enhancement of the laboratory quality system.
Insights
ISO/IEC 17025 accreditation significantly improved quality compliance in a Nigerian medicine testing laboratory. The study found fewer and less severe nonconformities after accreditation, enhancing the laboratory
Area of Science:
- Pharmaceutical Science
- Laboratory Quality Management
- Regulatory Science
Background:
- Quality compliance in medicine testing laboratories is crucial for reliable test reports.
- National Medicines Regulatory Authority (NMRA) laboratories play a vital role in public health.
- Accreditation to international standards like ISO/IEC 17025 presents challenges for low-income countries.
Purpose of the Study:
- To investigate the impact of ISO/IEC 17025 accreditation on the performance of a National Medicines Regulatory Authority Quality Control laboratory.
- To provide evidence of improved quality compliance in a low-resource setting.
- To assess if accreditation affects adherence to quality standards and reduces nonconformity severity.
Main Methods:
- Evaluated pre- and post-accreditation audits of nonconformities against ISO/IEC 17025:2005 standards.
- Analyzed management and technical requirements.
- Focused on a Quality Control laboratory within the National Agency for Food and Drug Administration and Control (NAFDAC) in Nigeria.
Main Results:
- A statistically significant decrease in the total number of nonconformities was observed post-accreditation (2013-2017 and 2013-2018).
- The severity of nonconformities and the number of major observations were reduced.
- Statistical analysis confirmed a significant positive impact of accreditation on quality compliance.
Conclusions:
- ISO/IEC 17025 accreditation led to a higher level of quality compliance in the NMRA Quality Control laboratory.
- Accreditation enhanced the reliability of medicine testing reports.
- The laboratory's overall quality system was significantly improved post-accreditation.
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