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This International Standard is the entry point of the whole suite of International Standards for software and systems product line engineering and management. The scope of this International Standard is to provide the terms...

Note: This notice of intent was withdrawn by the responsible SDO on June 20, 2023. Note: The standard development activity for this NOI (originally published on June 6, 2023) was updated by the responsible SDO on June 13...

This Standard covers requirements for control units, fire alarm systems and control unit accessories for use in accordance with the Standard for the Installation of Fire Alarm Systems, CAN/ULC-S524, in accordance with Rule 32...

1.1 Introduction 1.1.1 The purpose of this standard is to provide minimum requirements for the design, construction, and marking of electrical equipment or parts of such equipment for use in Class I and Class II, Division 2...

1.1 These requirements and methods of test apply to fire damper assemblies rated ¾ h, 1 h, 1½ h, 2 h, or 3 h for use in air-conditioning and ventilating system ducts or openings (without ducts) piercing horizontally or...

1.1 Purpose The purpose of this Standard is to provide a framework for consistent recording and classification of information on work-related injuries and diseases in Canada. Such information may be used to make comparisons...

HSO is developing a National Standard of Canada (NSC) outlining best practices for the co-design and delivery of an integrated, people-centred spinal cord injury (SCI) rehabilitation program. The CAN/HSO S3402:2022—...

These requirements cover electrically operated single and multiple station smoke alarms intended for open area protection in indoor locations, in accordance: a) Installation of Smoke Alarms, CAN/ULC-S553; b) National Building...

These requirements cover electrically operated single and multiple station smoke alarms intended for open area protection in indoor locations and portable smoke alarms used as "travel" alarms in accordance with: a)...

1.1 These requirements cover devices and systems intended for use in accordance with Annex A, Ref. No. 1, to reduce the risk of electric shock to the user from accessible parts, in grounded or isolated circuits for charging...

1.1 This part of ISO 11137 specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices. NOTE Although the scope of this part of ISO 11137 is limited to...

1.1 These requirements cover devices and systems intended for use in accordance with Annex A, Ref. No. 1, to reduce the risk of electric shock to the user from accessible parts, in grounded or isolated circuits for charging...