ISO/IEC 17025:2017 7 Process requirements 7.1 Review of requests, tenders and contracts 7.2 Selection, verification and validation of methods 7.3 Sampling 7.4 Handling of test or calibration items 7.5 Technical records 7.6 Evaluation of measurement uncertainty 7.7 Ensuring the validity of results 7.8 Reporting of results 7.9 Complaints. ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main ISO standard used by testing and calibration laboratories. In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent. ISO/IEC specifies the general requirements for the competence, impartiality and consistent operation of laboratories. This document is applicable to all organizations performing laboratory activities, regardless of the number of personnel.
ISO/IEC Working Document Instruction Page NOTES: 1. This working document is intended as a checklist for the assessor when conducting Testing and Calibration Laboratory and Sampling Organization Assessments according to ISO/IEC. This standard incorporates all elements of ISO 9001:2015 relevant to testing. The International Organization for Standardization (ISO) has released the most recent version of the ISO/IEC 17025 standard-the 2017 edition. The development of this standard became necessary as it is geared towards achieving the goal and purpose of promoting confidence, accuracy and trustworthiness in the operation of testing and calibration laboratories. ISO/IEC is applicable to all organizations performing laboratory activities, regardless of the number of personnel. Laboratory customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others use ISO/IEC in confirming or recognizing the competence of laboratories.
General requirements for the competence of testing and calibration laboratories (ISO/IEC 17025:2017); German and English version EN ISO/IEC 17025:2017 (Foreign Standard)
DIN EN ISO/IEC 17025 specifies the general requirements for the competence, impartiality and consistent operation of laboratories. This standard is applicable to all organizations performing laboratory activities, regardless of the number of personnel. Laboratory customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others use this standard in confirming or recognizing the competence of laboratories. DIN EN ISO/IEC 17025 has been developed with the objective of promoting confidence in the operation of laboratories. This document contains requirements for laboratories to enable them to demonstrate they operate competently, and are able to generate valid results. Laboratories that conform to this standard will also operate generally in accordance with the principles of ISO 9001. This document requires the laboratory to plan and implement actions to address risks and opportunities. Addressing both risks and opportunities establishes a basis for increasing the effectiveness of the management system, achieving improved results and preventing negative effects. The laboratory is responsible for deciding which risks and opportunities need to be addressed. The use of this standard will facilitate cooperation between laboratories and other bodies, and assist in the exchange of information and experience, and in the harmonization of standards and procedures. The acceptance of results between countries is facilitated if laboratories conform to this standard.
Content Provider Deutsches Institut für Normung [DIN]
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Complying With Iso 17025 2017
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Iso Iec 17025 2017 Standard Edition
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