- Report #: NT TR 569 Edition 4 Spanish
- Approved: April 2014
- Author(s): Håvard Hovind, Bertil Magnusson, Mikael Krysell, Ulla Lund, Irma Mäkinen
- Version: 4 – Spanish
According to ISO/IEC 17025 (3): The laboratory shall have quality control procedures for monitoring the validity of tests undertaken. The resulting data shall be recorded in such a way that trends are detectable and, where practicable, statistical techniques shall be applied to the reviewing of the results. The monitoring shall include e.g. regular use of internal quality control. … Quality control data shall be analysed and, where they are found to be outside pre-defined criteria, planned action shall be taken to correct the problem and to prevent incorrect results from being reported.
Internal quality control at the chemical analytical laboratory, involves a continuous, critical evaluation of the laboratory’s own analytical methods and working routines. The control encompasses the analytical process starting with the sample entering the laboratory and ending with the analytical report. The most important tool in this quality control is the use of control charts. The basis is that the laboratory runs control samples together with the routine samples.
The results of the control program may be used in several ways – the analyst will have an important quality tool in his/her daily work, the customer can get an impression of the laboratory’s quality and the laboratory can use the results in the estimation of the measurement uncertainty.
The QC has to be part of a quality system and should be formally reviewed on a regular basis. The aim of this handbook is to describe a fit for purpose system for internal quality control at analytical laboratories that are performing chemical analysis. The approach is general, but the examples are mainly from environmental analyses.
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