Benefits:-

  • Increase of confidence in Testing/ Calibration data and of personnel performing work.

  • Better control of laboratory operations and feedback to laboratories

  • Potential increase in business due to enhanced customer confidence and satisfaction.

  • Customers can search and identify the laboratories accredited by The Accreditation Member Body for their specific requirements from their website or Directory of Accredited Laboratories.

  • Users of accredited laboratories will enjoy greater access for their products, in both domestic and international markets, when tested by accredited laboratories.

  • Savings in terms of time and money due to reduction or elimination of the need for re-testing of products.

  • Improved national and global reputation and image of the laboratory.

  • Continually improving data quality and laboratory effectiveness.

ISO/IEC 17025

 

General requirements for the competence of testing and calibration laboratories

 

Originally known as ISO/IEC Guide 25, ISO/IEC 17025 was initially issued by the International Organiszation for Standardization in 1999. There are many commonalities with the ISO 9001 standard, but ISO/IEC 17025 is more specific in requirements for competence. And it applies directly to those organizations that produce testing and calibration results. Since its initial release, a second release was made in 2005 after it was agreed that it needed to have its quality system words more closely aligned with the 2000 version of ISO 9001.

 

The standard was first published in 1999 and on 12 May 2005 the alignment work of the ISO/CASCO committee responsible for it was completed with the issuance of the reviewed standard. The most significant changes introduced greater emphasis on the responsibilities of senior management, and explicit requirements for continual improvement of the management system itself, and particularly, communication with the customer.

 

The contents of ISO/IEC 17025 – The ISO/IEC 17025 standard itself comprises five elements that are Scope, Normative References, Terms and Definitions, Management Requirements and Technical Requirements. The two main sections in ISO/IEC 17025 are Management Requirements and Technical Requirements. Management requirements are primarily related to the operation and effectiveness of the quality management system within the laboratory. Technical requirements includes factors which determines the correctness and reliability of the tests and calibrations performed in laboratory.

 

Laboratories use ISO/IEC 17025 to implement a quality system aimed at improving their ability to consistently produce valid results.

It is also the basis for accreditation from an accreditation body. Since the standard is about competence, accreditation is simply formal recognition of a demonstration of that competence. A prerequisite for a laboratory to become accredited is to have a documented quality management system. The usual contents of the quality manual follow the outline of the ISO/IEC 17025 standard.

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