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Developing laboratory capacity for Good Laboratory Practice certification: lessons from a Tanzanian insecticide testing facility
Background: With increasing insecticide resistance in malaria-endemic countries there is an urgent need for safe and effective novel vector control products. To improve the capacity of facilities that test insecticides in sub-Saharan Africa, a programme is supporting seven facilities towards Good La...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399503/ https://www.ncbi.nlm.nih.gov/pubmed/32789289 http://dx.doi.org/10.12688/gatesopenres.13133.1 |
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author | Begg, Sara Wright, Alexandra Small, Graham Mosha, Franklin Kirby, Matthew Snetselaar, Janneke Aziz, Salum Bharmal, Jameel Dacombe, Russell Bates, Imelda |
author_facet | Begg, Sara Wright, Alexandra Small, Graham Mosha, Franklin Kirby, Matthew Snetselaar, Janneke Aziz, Salum Bharmal, Jameel Dacombe, Russell Bates, Imelda |
author_sort | Begg, Sara |
collection | PubMed |
description | Background: With increasing insecticide resistance in malaria-endemic countries there is an urgent need for safe and effective novel vector control products. To improve the capacity of facilities that test insecticides in sub-Saharan Africa, a programme is supporting seven facilities towards Good Laboratory Practice (GLP) certification, the globally recognized standard for quality management system (QMS) for the conduct of non-clinical and environmental studies. The World Health Organization (WHO) GLP Handbook provides guidance on a stepwise approach to implement a GLP compliant QMS. This study assesses auditor GLP checklists and timings outlined in the WHO GLP Handbook in the real-life context of a Tanzanian insecticide-testing facility, evaluating their implementation in this context. Methods and Principle Findings: We conducted document review and semi-structured interviews with staff at all levels of the test facility to explore factors that influenced progress towards GLP certification. We found that while auditor GLP checklists underemphasised computer systems, they were otherwise broadly applicable. Factors that delayed time to completion of GLP certification included the need for extensive infrastructure improvements, the availability of regional expertise related to GLP, the capacity of national and regional external systems and services to meet GLP compliance requirements, and training development required for Standard Operating Procedure implementation. Conclusion: The standards required for full GLP compliance are rigorous, with an expected completion timeline to implementation of 24 months. This study shows that in low and middle-income countries this timeline may be unrealistic due to challenges related to infrastructure development and lack of regional capacity and expertise. We recommend a comprehensive gap analysis when starting a project, including these areas which are beyond those recommended by the WHO GLP Handbook. These challenges can be successfully overcome and the experience in Tanzania provides key lessons for other facilities seeking GLP certification or the development of similar QMS. |
format | Online Article Text |
id | pubmed-7399503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-73995032020-08-11 Developing laboratory capacity for Good Laboratory Practice certification: lessons from a Tanzanian insecticide testing facility Begg, Sara Wright, Alexandra Small, Graham Mosha, Franklin Kirby, Matthew Snetselaar, Janneke Aziz, Salum Bharmal, Jameel Dacombe, Russell Bates, Imelda Gates Open Res Research Article Background: With increasing insecticide resistance in malaria-endemic countries there is an urgent need for safe and effective novel vector control products. To improve the capacity of facilities that test insecticides in sub-Saharan Africa, a programme is supporting seven facilities towards Good Laboratory Practice (GLP) certification, the globally recognized standard for quality management system (QMS) for the conduct of non-clinical and environmental studies. The World Health Organization (WHO) GLP Handbook provides guidance on a stepwise approach to implement a GLP compliant QMS. This study assesses auditor GLP checklists and timings outlined in the WHO GLP Handbook in the real-life context of a Tanzanian insecticide-testing facility, evaluating their implementation in this context. Methods and Principle Findings: We conducted document review and semi-structured interviews with staff at all levels of the test facility to explore factors that influenced progress towards GLP certification. We found that while auditor GLP checklists underemphasised computer systems, they were otherwise broadly applicable. Factors that delayed time to completion of GLP certification included the need for extensive infrastructure improvements, the availability of regional expertise related to GLP, the capacity of national and regional external systems and services to meet GLP compliance requirements, and training development required for Standard Operating Procedure implementation. Conclusion: The standards required for full GLP compliance are rigorous, with an expected completion timeline to implementation of 24 months. This study shows that in low and middle-income countries this timeline may be unrealistic due to challenges related to infrastructure development and lack of regional capacity and expertise. We recommend a comprehensive gap analysis when starting a project, including these areas which are beyond those recommended by the WHO GLP Handbook. These challenges can be successfully overcome and the experience in Tanzania provides key lessons for other facilities seeking GLP certification or the development of similar QMS. F1000 Research Limited 2020-06-12 /pmc/articles/PMC7399503/ /pubmed/32789289 http://dx.doi.org/10.12688/gatesopenres.13133.1 Text en Copyright: © 2020 Begg S et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Begg, Sara Wright, Alexandra Small, Graham Mosha, Franklin Kirby, Matthew Snetselaar, Janneke Aziz, Salum Bharmal, Jameel Dacombe, Russell Bates, Imelda Developing laboratory capacity for Good Laboratory Practice certification: lessons from a Tanzanian insecticide testing facility |
title | Developing laboratory capacity for Good Laboratory Practice certification: lessons from a Tanzanian insecticide testing facility |
title_full | Developing laboratory capacity for Good Laboratory Practice certification: lessons from a Tanzanian insecticide testing facility |
title_fullStr | Developing laboratory capacity for Good Laboratory Practice certification: lessons from a Tanzanian insecticide testing facility |
title_full_unstemmed | Developing laboratory capacity for Good Laboratory Practice certification: lessons from a Tanzanian insecticide testing facility |
title_short | Developing laboratory capacity for Good Laboratory Practice certification: lessons from a Tanzanian insecticide testing facility |
title_sort | developing laboratory capacity for good laboratory practice certification: lessons from a tanzanian insecticide testing facility |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399503/ https://www.ncbi.nlm.nih.gov/pubmed/32789289 http://dx.doi.org/10.12688/gatesopenres.13133.1 |
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