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CAN/CSA-C22.2 NO. 60601-1:14 + A2:22 (R2022) (CONSOLIDATED) – Medical electrical equipment – Part 1: General requirements for basic safety and essential performance (Adopted IEC 60601-1:2005, edition 3:2005 consolidated with amendment 1:2012 and amendment 2:2020, with Canadian deviations) | Appareils électromédicaux – Partie 1: Exigences générales pour la sécurité de base et les performances essentielles (norme IEC 60601-1:2005 adoptée, édition 3:2005 consolidée par l’amendement 1:2012 et l’amendement 2:2020, avec exigences propres au Canada)

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CAN/CSA-C22.2 NO. 60601-1:14 (R2022) – Medical electrical equipment – Part 1: General requirements for basic safety and essential performance (Adopted IEC 60601-1:2005, third edition, 2005-12, including amendment 1:2012, with Canadian deviations) | Appareils électromédicaux – Partie 1: Exigences générales pour la sécurité de base et les performances essentielles (norme CEI 60601-1:2005 adoptée, troisième édition, 2005-12, y compris l’amendment 1:2012, avec exigences propres au Canada)

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1448

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CSA C22.2 NO. 60529:16 (R2026) – Degrees of protection provided by enclosures (IP Code) (Adopted IEC 60529:1989, edition 2:1989 consolidated with amendment 1:1999 and amendment 2:2013, with Canadian deviations) | Degrés de protection procurés par les enveloppes (Code IP) (norme IEC 60529:1989 adoptée , édition 2:1989 consolidée par l’amendement 1:1999 et l’amendement 2:2013, avec exigences propres au Canada)

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307

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CSA C22.2 NO. 60601-1-11:15 + A1:20 (CONSOLIDATED) (R2025) – Medical electrical equipment – Part 1-11: General requirements for basic safety and essential performance – Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment (Adopted IEC 60601-1-11:2015, edition 2:2015 consolidated with amendment 1:2020, with Canadian deviations) | Appareils électromédicaux – Partie 1-11 : Exigences générales pour la sécurité de base et les performances essentielles – Norme collatérale : Exigences pour les appareils électromédicaux et les systèmes électromédicaux utilisés dans l’environnement des soins à domicile (norme IEC 60601-1-11:2015 adoptée, édition 2:2015 consolidée par l’amendement 1:2020, avec exigences propres au Canada)

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CSA C22.2 NO. 60598-2-18:25 – Luminaires — Part 2-18: Particular requirements — Luminaires for swimming pools and similar applications (Adopted IEC 60598-2-18:2022, third edition, 2022-08, with Canadian deviations) | Luminaires — Partie 2-18 : Exigences particulières — Luminaires pour piscines et usages analogues (norme IEC 60598-2-18:2022 adoptée, troisième édition, 2022-08, avec exigences propres au Canada)

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205

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CAN/CSA-C22.2 NO. 60601-1:14/A2:22 (R2022) – Amendment 2:2022 to CAN/CSA-C22.2 NO. 60601-1:14, Medical electrical equipment – Part 1: General requirements for basic safety and essential performance (Adopted amendment 2:2020 to IEC 60601-1:2005, with Canadian deviations) | Modification 2:2022 à CAN/CSA-C22.2 NO. 60601-1:14, Appareils électromédicaux – Partie 1: Exigences générales pour la sécurité de base et les performances essentielles (amendement 2:2020 adoptée à la norme CEI 60601-1:2005, avec exigences propres au Canada)

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608

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CSA C22.2 NO. 60601-1-10:09 (R2025) – Medical electrical equipment – Part 1-10: General requirements for basic safety and essential performance – Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted IEC 60601-1-10:2007, first edition, 2007-11) | Appareils électromédicaux – Partie 1-10: Exigences générales pour la sécurité de base et les performances essentielles – Norme collatérale: Exigences pour le développement des régulateurs physiologiques en boucle fermée (norme IEC 60601-1-10:2007 adoptée, première édition, 2007-11)

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331

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CSA C22.2 NO. 60601-1-10:09 + A1:14 (R2020) + A2:21 (CONSOLIDATED) – Medical electrical equipment — Part 1-10: General requirements for basic safety and essential performance — Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted IEC 60601-1-10:2007, edition 1:2007 consolidated with amendment 1:2013 and amendment 2:2020, with Canadian deviations) | Appareils électromédicaux — Partie 1-10 : Exigences générales pour la sécurité de base et les performances essentielles — Norme collatérale : Exigences pour le développement des régulateurs physiologiques en boucle fermée (norme IEC 60601-1-10:2007 adoptée, édition 1:2007 consolidée par l’amendement 1:2013 et l’amendement 2:2020, avec exigences propres au Canada)

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CSA C22.2 No. 60601-1-10:09/A1:14 (R2025) – Amendment 1:2014 to CSA C22.2 NO. 60601-1-10:09, Medical electrical equipment – Part 1-10: General requirements for basic safety and essential performance – Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted amendment 1:2013 to IEC 60601-1-10:2007) | Modification 1:2014 à CSA C22.2 NO. 60601-1-10:09, Appareils électromédicaux – Partie 1-10: Exigences générales pour la sécurité de base et les performances essentielles – Norme collatérale: Exigences pour le développement des régulateurs physiologiques en boucle fermée (Amendement 1:2013 adoptée de la norme IEC 60601-1-10:2007)

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29

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CSA C22.2 NO. 60601-1-10B:09 – Amendment 2:2021 to CSA C22.2 NO. 60601-1-10:09, Medical electrical equipment – Part 1-10: General requirements for basic safety and essential performance – Collateral Standard: Requirements for the development of physiologic closed-loop controllers (Adopted amendment 2:2020 to IEC 60601-1-10:2007) | Modification 2:2021 à CSA C22.2 NO. 60601-1-10:09, Appareils électromédicaux – Partie 1-10: Exigences générales pour la sécurité de base et les performances essentielles – Norme collatérale: Exigences pour le développement des régulateurs physiologiques en boucle fermée (Amendement 2:2020 adoptée de la norme IEC 60601-1-10:2007)

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84

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ISO 17025:2017

ISO 17025:2017 General requirements for the competence of testing and calibration laboratories

CDN $333.00

SKU: 5c9a574921cd Category:

Description

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.

Edition

3

Published Date

2017-11-29

Status

PUBLISHED

Pages

30

Language Detail Icon

English

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Abstract

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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