ISO/IEC 17025:2017 specifies the general requirements for the competence, impartiality and consistent operation of laboratories.
ISO/IEC 17025:2017 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 17025:2017 in confirming or recognizing the competence of laboratories.

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This document specifies general requirements for sampling, preservation, handling, transport and storage of all water samples including those for biological analyses.
It is not applicable to water samples intended for microbiological analyses as specified in ISO 19458, ecotoxicological assays, biological assays and passive sampling as specified in the scope of ISO 5667‑23.
This document is particularly appropriate when spot or composite samples cannot be analysed on site and have to be transported to a laboratory for analysis.

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ISO/IEC 17043:2010 specifies general requirements for the competence of providers of proficiency testing schemes and for the development and operation of proficiency testing schemes. These requirements are intended to be general for all types of proficiency testing schemes, and they can be used as a basis for specific technical requirements for particular fields of application.

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ISO 13528:2015 provides detailed descriptions of statistical methods for proficiency testing providers to use to design proficiency testing schemes and to analyse the data obtained from those schemes. It provides recommendations on the interpretation of proficiency testing data by participants in such schemes and by accreditation bodies. The procedures in ISO 13528:2015 can be applied to demonstrate that the measurement results obtained by laboratories, inspection bodies, and individuals meet specified criteria for acceptable performance. ISO 13528:2015 is applicable to proficiency testing where the results reported are either quantitative measurements or qualitative observations on test items.

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Frequently Asked Questions

An EU Regulation is a binding legislative act that must be applied in its entirety across the European Union. Unlike directives, regulations do not need to be transposed into national law and are directly applicable in all member states. Regulations are used when uniform application across all EU countries is essential.

Slovenian Regulation 2021-01-0307 covers "Pravilnik o obratovalnem monitoringu stanja podzemne vode". There are 4 standards associated with this slovenian regulation.

Harmonized standards under 2021-01-0307 are European standards (ENs) developed by CEN, CENELEC, or ETSI in response to a mandate from the European Commission. When these standards are cited in the Official Journal of the European Union, products manufactured in conformity with them benefit from a presumption of conformity with the essential requirements of 2021-01-0307, facilitating CE marking and free movement within the European Economic Area.

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