Rechercher

This National Standard of Canada is equivalent to International Standard CEI/IEC 1010-2-051:1995. 1. Scope and object This clause of part 1 is appicable except as follows: 1.1 Scope Replacement: This part 2 is appicable to electrically operated laboratory equipment and its accessoires for mechanical mixing and stirring, where mechanical energy influences the shape or size or…

This National Standard of Canada is equivlent to International Standard IEC 61010-2-051:2003, second edition. 1 Scope and object This clause of Part 1 is applicable except as follows: 1.1 Scope Replacement: Replace the whole text by the following new paragraph: This part of IEC 61010 is applicable to electrically operated laboratory equipment and its accessories for mechanical mixing and…

This document specifies the requirements for competence to carry out reference measurement procedures in laboratory medicine, using the requirements of ISO/IEC 17025:2017 as a normative reference and listing additional requirements for calibration laboratories to perform their tasks adequately. The relationship between clauses in this document and ISO/IEC 17025:2017 are summarized in Annex A.…

ISO/IEC 17025:2005 specifies the general requirements for the competence to carry out tests and/or calibrations, including sampling. It covers testing and calibration performed using standard methods, non-standard methods, and laboratory-developed methods. It is applicable to all organizations performing tests and/or calibrations. These include, for example, first-, second- and third-party…

ISO/IEC 17025:2005 specifies the general requirements for the competence to carry out tests and/or calibrations, including sampling. It covers testing and calibration performed using standard methods, non-standard methods, and laboratory-developed methods. It is applicable to all organizations performing tests and/or calibrations. These include, for example, first-, second- and third-party…

ISO 15189:2012 specifies requirements for quality and competence in medical laboratories. ISO 15189:2012 can be used by medical laboratories in developing their quality management systems and assessing their own competence. It can also be used for confirming or recognizing the competence of medical laboratories by laboratory customers, regulating authorities and accreditation bodies.

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…

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…

1. Scope 1.1 This Standard provides requirements for polyolefin laboratory drainage systems from corrosive applications. Requirements for materials, pipe, and fittings are included. Note: Polyolefin includes both polyethylene and polypropylene plastics. 1.2 These requirements apply to pipe and fittings that are to be joined by heat fusion using the joining equipment supplied by the…

This document specifies requirements for quality and competence in medical laboratories. This document is applicable to medical laboratories in developing their management systems and assessing their competence. It is also applicable for confirming or recognizing the competence of medical laboratories by laboratory users, regulatory authorities and accreditation bodies. This document is also…