What Is The Iso 17025 And How Is Iso 17025 Certification Beneficial To The Organization?

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ISO/IEC 17025 standard is especially for the general requirements for the competence, impartiality, and consistent operation of laboratories. ISO/IEC 17025 is valid to all organizations performing laboratory activities, irrespective of the number of employees. Laboratory clients, monitoring authorities, organizations, and schemes using peer-assessment, accreditation bodies, and others use ISO/IEC 17025 in confirmative or recognizing the competence of laboratories.

What is the ISO 17025 standard?

ISO 17025 is an international standard developed by ISO (International Organization for Standardization) and the International Electrotechnical Commission (IEC) under the coordination of the ISO Conformity Assessment Committee (CASCO), which establishes the requirements that testing and calibration laboratories must meet. Besides, this standard provides the requirements to be met by testing and calibration laboratories, facilitating the harmonization of quality criteria. ISO/IEC 17025 is convenient for any organization that performs testing, sampling, or calibration and wants reliable results of any size and any type. ISO ...
... 17025 includes all types of laboratories, whether they be owned and operated by government, industry, or, in fact, any other organization. The ISO 17025 standard is also important for the universities, research canter, governments’ labs, inspection bodies, product certification organizations, and other conformity assessment bodies who need to do testing, sampling, or calibration.

What are the benefits of the ISO 17025 standard?

The ISO 17025 standard helps to increases the trustworthiness of test results generated by the laboratory. It also creates technical competency in the event of speculation and/or validity issues. The ISO 17025 standard helps to increases the productivity of the laboratory and the customer complaints are reduced. So, the laboratory raises a strong competitive edge, and the working expenses are reduced. The guideline enables traceability of measurements and calibrations to optimum standards, creates the technical skill of staff, keeps a record of test equipment, also ensures the accuracy of test results, validity and correctness of test and calibration methods, appropriate handling and movement of test items, and the quality of the testing environment and sampling. It helps to increases systematic approach, improves the lab testing environment, reduces lab waste, improves customers’ satisfaction level, and cost reduction.

What are the requirements of the ISO 17025 standard?

•Recommend one person as Management Representative for establishing, implementation, and monitoring of the effective implementation of the management system's necessities and one person as technical manager for establishing implementation, and monitoring of the effective implementation of the technical requirements.
•Examination constraint, its location of performance, the field of inspection, type and range of inspection, and reference of proven inspection methods.
•Analysis of re-inspection outcomes statistically.
•Comparison with other accredited inspection bodies to check the level of competence against other ISO/IEC 17025 accredited inspection bodies, based on statistical analysis.

What is the ISO/IEC 17025:2017 Documentation Requirements?

During the certification, the following are the documents that should be required to maintain in daily practices for any testing and calibration laboratories.
•ISO 17025 Manual: ISO 17025 manual with the quality policy and each chapter is explaining and macro-level management strategy and commitment and how the laboratory system is implemented.
•ISO 17025 Procedures: Certain mandatory procedures should be maintained while used for the implementation of the system in the testing laboratory and compliance with accreditation standard requirements covering mandatory requirements of documented information.
•Exhibits: The exhibits including exhibits for calibration periodicity of every instrument that is used in the laboratory should maintain.
•Standard Operating Procedures: These are the records known as SOPs for good work practices in the testing and calibration laboratories are also in the list of mandatory documented information.