Implementation of Quality in Testing Laboratories (ISO/IEC 17025:2017)

Authors

DOI:

https://doi.org/10.5377/ribcc.v9i17.15150

Keywords:

quality in testing laboratories, risk management, system LIMS, lab setting

Abstract

The research aims to briefly describe how to implement the requirements established in the ISO/IEC 17025:2017 standard, for the competence of quality testing laboratories, highlighting the context of the Laboratory and the basic elements of risk according to the guidelines. of the ISO 31000:2018 standard. It begins with a historical review of the evolution of quality and its importance in testing laboratories, describing the basic components of the laboratory context, emphasizing external and internal factors. The necessary aspects of risk management summarized through a flowchart are addressed, highlighting risk identification, analysis, assessment and treatment. Then a brief description of the requirements for competitiveness of laboratories is made, prioritizing the process approach and risk management that is explicitly found throughout the content of the standard. Finally, the importance of using the Laboratory Information Management System (LIMS) and artificial intelligence is discussed, as a tool to guarantee productivity and quality in customer results.

 

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Author Biographies

G. Delgado, National Autonomous University of Nicaragua, Leon. Nicaragua

Retired researcher UNAN Leon

Jairo Salazar-Casco, National Autonomous University of Nicaragua, Leon. Nicaragua

Research Assistant Vice President for Research, Innovation and Entrepreneurship, UNAN Leon

Degree in Chemistry from UNAN-León

Master in Biotechnology from the University of Extremadura, Spain

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Published

2023-03-22

How to Cite

Delgado, G., & Salazar-Casco, J. (2023). Implementation of Quality in Testing Laboratories (ISO/IEC 17025:2017). Rev. Iberoam. Bioecon. Cambio Clim., 9(17), 2029–2047. https://doi.org/10.5377/ribcc.v9i17.15150

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Section

Biothecnology Aplication

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