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This is the first edition of CAN/CSA-ISO 10012, Measurement management systems - Requirements for measurement processes and measuring equipment, which is an adoption without modification of the identically titled ISO...

1.1 This Standard specifies the requirements for low-halogen aboveground (Type AG) reinforced thermosetting resin conduit (RTRC) and fittings for installation and use in accordance with CSA C22.1, Canadian Electrical Code...

1.1 This Standard specifies the requirements for low-halogen aboveground (Type AG) reinforced thermosetting resin conduit (RTRC) and fittings for installation and use in accordance with CSA C22.1, Canadian Electrical Code...

Health Standards Organization (HSO) is developing a National Standard of Canada (NSC) for Home Care and Support Services, CAN/HSO 35001:2025. This standard will focus on enabling high-quality, people-centered care in the home...

1.1 This Standard applies to single-polarity, hand-, or tool-applied splicing wire and cable connectors intended for use with all alloys of copper, aluminum conductors, or copper-clad aluminum conductors, or all three, in...

1.1 This Standard applies to the overhead contact system and traction power supply to the locomotive, using a single-phase alternating supply at 25 or 50 kV nominal voltage, 60 Hz. 1.2 This Standard has been written primarily...

Please note the following NOI has been withdrawn on 2019-02-12 as requested by the responsible SDO. This National Standard of Canada applies to flammability performance requirements for patient apparel, mattresses, bed linen...

This document gives the safety requirements and measures to reduce risks related to woodworking machines arising during operation, adjustment, maintenance, transport, assembly, dismantling, disabling and scrapping and which...

Standard specification for laboratory testing, performance assessment, and health effects evaluation of microplastics and nanoplastics originating from plumbing, water treatment and distribution, food-service equipment, and...

This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of non-critical medical devices not intended to be sterilized (i.e. a medical device that is...