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Contact: [email protected] (Ron Meyers )
Origin: CSA
Close date: Jun 9, 2026
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1.1 General

This Standard provides core competency requirements for GSAR operations for the four core roles of searcher, team leader, SAR manager and canine handler .

1.2 Purpose

This Standard was developed to provide a foundation for interoperability and portability of GSAR skills within Canada. It is intended to facilitate training curriculum development and professional development planning so that competence is maintained and enhanced.

This Standard is an important tool for documenting and communicating the knowledge, skills, and abilities for those involved in GSAR operations and for evaluating performance. It provides a reference tool for multiple stakeholders and presents a starting point for meaningful discussion about the future direction of GSAR in Canada.

1.3 Terminology

In this Standard, “shall” is used to express a requirement, i.e., a provision that the user is obliged to satisfy in order to comply with the Standard; “should” is used to express a recommendation or that which is advised but not required; and “may” is used to express an option or that which is permissible within the limits of the Standard.

Notes accompanying clauses do not include requirements or alternative requirements; the purpose of a note accompanying a clause is to separate from the text explanatory or informative material.

Notes to tables and figures are considered part of the table or figure and may be written as requirements.

Annexes are designated normative (mandatory) or informative (non-mandatory) to define their application.

Contact: [email protected] (Ron Meyers )
Origin: CSA
Close date: Jun 9, 2026
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1.1 Généralités

La présente norme définit les compétences de base requises pour les opérations de RSS pour les quatre rôles principaux que sont le chercheur, le chef d’équipe et le gestionnaire des opérations de R-S et le maître-chien.

1.2 But

La présente norme a été élaborée pour fournir un fondement à l’interopérabilité et à la transférabilité des habiletés en RSS à l’intérieur du Canada. Elle est destinée à faciliter l’élaboration des programmes de formation et la planification du perfectionnement professionnel afin de maintenir et d’améliorer les compétences.

La présente norme est un outil important pour documenter et communiquer les connaissances, les aptitudes et les capacités des personnes participant aux opérations de RSS et pour évaluer les performances. Elle constitue un outil de référence pour divers intéressés, ainsi qu’un point de départ pour des discussions éclairées sur les orientations futures de RSS au Canada.

1.3 Terminologie

Dans la présente norme, le terme « doit » indique une exigence, c’est-à-dire une prescription que l’utilisateur est obligé de respecter pour assurer la conformité à la norme; « devrait » indique une recommandation ou ce qu’il est conseillé, mais non obligatoire de faire; et « peut » indique une possibilité ou ce qu’il est permis de faire en fonction des limites de la norme.

Les notes qui accompagnent les articles ne comprennent pas de prescriptions ni de recommandations. Elles servent à séparer du texte les explications ou les renseignements qui ne font pas proprement partie de la norme.

Les notes au bas des figures et des tableaux font partie de ceux-ci et peuvent être rédigées comme des prescriptions.

Les annexes sont qualifiées de normatives (obligatoires) ou d’informatives (facultatives) pour en préciser l’application.

Categories: Electrical
Contact: [email protected] (Yi Wang)
Origin: CSA
Close date: Jun 10, 2026
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CSA Scope

201.1.1 *Scope
[Add the following paragraph]
This Standard applies to ME EQUIPMENT and ME SYSTEMS that are intended to be installed or used in accordance with CSA C22.1, Canadian Electrical Code, Part I.

IEC Scope

Clause 1 of the general standard1 applies, except as follows:

 

201.1.1 * Scope

 

Replacement:

 

This part of the 80601 International Standard applies to BASIC SAFETY and ESSENTIAL PERFORMANCE requirements of MULTIFUNCTION PATIENT MONITORS as defined in 201.3.201, hereafter referred to as ME EQUIPMENT or MEDICAL ELECTRICAL SYSTEMS. This particular standard applies to MULTIFUNCTION PATIENT MONITORS intended for use in professional healthcare facilities as well as in the EMERGENCY MEDICAL SERVICE ENVIRONMENT or the HOME HEALTHCARE ENVIRONMENT.

 

The scope of this document is restricted to ME EQUIPMENT or MEDICAL ELECTRICAL SYSTEMS intended for connection to a single PATIENT that has two or more PHYSIOLOGICAL MONITORING UNITS.

 

NOTE For purposes of this document, a pregnant mother and her fetus(es) are considered a single PATIENT.

 

This document does not specify requirements for individual PHYSIOLOGICAL MONITORING UNITS such as ECG, invasive pressure and pulse oximetry. The particular standards related to these PHYSIOLOGICAL MONITORING UNITS specify requirements from the perspective of stand-alone ME EQUIPMENT. This particular standard addresses the additional requirements related to MULTIFUNCTION PATIENT MONITORS.MULTIFUNCTION PATIENT MONITORS can be integrated into other ME EQUIPMENT or MEDICAL ELECTRICAL SYSTEMS. When this is the case, other relevant standards also apply.

 

EXAMPLE 1 MULTIFUNCTION PATIENT MONITOR incorporated into a critical care ventilator where ISO 80601-2-12 also applies.

 

EXAMPLE 2 MULTIFUNCTION PATIENT MONITOR incorporated into a homecare ventilator for dependent PATIENT where ISO 80601-2-72 also applies.

 

EXAMPLE 3 MULTIFUNCTION PATIENT MONITOR incorporated into anesthetic workstation where ISO 80601-2-13 also applies.

 

EXAMPLE 4 MULTIFUNCTION PATIENT MONITOR incorporated into haemodialysis equipment, IEC 60601-2-16 also applies.

 

This document does not apply to implantable parts of MULTIFUNCTION PATIENT MONITORS.

Categories: Electrical
Contact: [email protected] (Yi Wang)
Origin: CSA
Close date: Jun 10, 2026
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CSA Scope

201.1.1 *Scope
[Add the following paragraph]
This Standard applies to ME EQUIPMENT and ME SYSTEMS that are intended to be installed or used in accordance with CSA C22.1, Canadian Electrical Code, Part I.

 

ISO Scope:

IEC 60601-1:2005+Amd 1:2012+Amd 2:2020, Clause 1 applies, except as follows:

 

201.1.1 *Scope

 

IEC 60601-1:2005+Amd 1:2012+Amd 2:2020, 1.1 is replaced by:

 

This document specifies particular requirements for the BASIC SAFETY and ESSENTIAL PERFORMANCE of a RESPIRATORY GAS MONITOR (RGM), hereafter referred to as ME EQUIPMENT, intended for CONTINUOUS OPERATION for use with a PATIENT.

 

This document specifies requirements for

 

— anaesthetic gas monitoring,

 

— carbon dioxide monitoring, and

 

— oxygen monitoring.

 

NOTE 1 An RGM can be either stand-alone ME EQUIPMENT or integrated into other equipment, e.g. an anaesthetic workstation or a ventilator.

 

This document is not applicable to an RGM intended for use with flammable anaesthetic agents.

 

If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

 

HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this document are not covered by specific requirements in this document except in IEC 60601-1:2005+Amd 1:2012+Amd 2:2020, 7.2.13 and 8.4.1.

 

NOTE 2 Additional information can be found in IEC 60601-1:2005+Amd 1:2012+Amd 2:2020, 4.2.

Origin: CSA
Close date: Jun 11, 2026
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1   Scope:

This document specifies the design, construction, type testing, and marking requirements for pressure regulators (as defined in 3.18) intended for the administration of medical gases and their mixtures in the treatment, management, diagnostic evaluation and care of patients or for gases used for driving surgical tools.


Examples of gases include oxygen, medical air and oxygen/nitrous oxide mixtures.


This document applies to pressure regulators:
a) intended to be connected to cylinders by the operator;
b) with integral flow-metering devices intended to be connected to cylinders by the operator;
 

A pressure regulator can be provided with pressure outlet or flow outlet, and can be adjustable or pre-set.
 

Pressure Regulators are intended to be fitted to refillable cylinders with a working pressure up to 30 000 kPa ( 300 bar) and can be provided with devices which control and measure the flow of the medical gas delivered.

Contact: [email protected] (Mark McEwen)
Origin: CSA
Close date: Jun 12, 2026
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Draft Amendment to C22.1

Origin: CSA
Close date: Jun 14, 2026
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1 Scope

1.1 General

This Standard specifies special requirements for the durability aspects of the design and construction of new parking structures and parts of buildings subject to vehicular traffic.

This includes pedestrian traffic areas adjoining to or contained within parking structures. These include areas such as stairs, and pedestrian bridges from parking structures.

The application of this Standard includes structures which are designed for the storage and/or repair of vehicles whether those structures are stand alone, above ground or below ground, part of or connected to the structure of a larger structure/development.

Note: This includes commercial, residential, industrial or institutional, and all other building types.

1.2 Structure types

New parking structures constructed of structural steel, reinforced concrete (including prestressed concrete), or a combination of these materials fall within the scope of this Standard.

1.3 Repair of existing parking structures

This Standard does not cover the repair of existing parking structures, and the provisions of this Standard are not necessarily appropriate for the repair and protection of existing structures.

Note: See CSA S448.1 for information on the repair of concrete structures.

1.4 Reference standards

In the event of conflict between this Standard and the reference standards, this Standard takes precedence.

1.5 Terminology

In this Standard, “shall” is used to express a requirement, i.e., a provision that the user is obliged to satisfy in order to comply with the Standard; “should” is used to express a recommendation or that which is advised but not required; “may” is used to express an option or that which is permissible within the limits of the Standard.

Notes accompanying clauses do not include requirements or alternative requirements; the purpose of a note accompanying a clause is to separate from the text explanatory or informative material.

Notes to tables and figures are considered part of the table or figure and may be written as requirements.

Annexes are designated normative (mandatory) or informative (non-mandatory) to define their application.

Categories: ANSI BSR8
Origin:
Close date: Jun 15, 2026
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CSA ISO 27914 has been posted for ANSI BSR-8 (ANSI Public Review) on the ANSI Standards Action Website. For further information please visit: https://www.ansi.org/resource-center/standards-action

Categories: Electrical
Contact: [email protected] (Matthew Wong)
Origin: CSA
Close date: Jun 16, 2026
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1.1 These requirements apply to DC conductive charging equipment intended to be supplied with a maximum input voltage of 1000 V ac or 1500 V dc, for recharging the propulsion batteries in over-the-road electric vehicles (EV). Equipment is intended to be installed in accordance with the Installation Codes in Annex A, Ref. No. 1. DC charging equipment, either standalone chargers or dispensers, with internal batteries exceeding 100 Wh and less than 20kWh serving as energy storage also is intended to be installed in accordance with the installation requirements in Annex A, Ref. No. AA. DC charging equipment with separable enclosures with internal batteries not in a standalone charger or charging dispenser shall be dual listed with the enclosures containing internal batteries also listed under UL 9540. DC charging equipment for EV installations are intended for either:

a) Dry location only, or

b) Dry, wet, and damp location.

 

1.2 The output of the DC charging equipment for EV covered by this standard does not exceed 1500 V dc.

 

1.3 For the purposes of this Standard, the term "electric vehicle", designated throughout by the initials "EV", is considered to cover electric vehicles, hybrid electric vehicles, and plug-in versions of these vehicles.

 

1.4 DC charging equipment for EV that is not a complete assembly and depends upon installation in an end product for compliance with the requirements in this Standard is investigated under the requirements of this Standard and the standard for the end product.

 

1.5 These requirements do not cover battery chargers covered by Annex A, Ref. Nos. 2 and 3.

 

1.6 These requirements do not cover on-board chargers.

 

1.7 These requirements do not cover electric vehicle supply equipment covered by Annex A, Ref. No. 4.

 

1.8 These requirements do not cover DC charging equipment for EV intended to be used in hazardous locations, such as near fuel dispensing stations.

 

1.9 These requirements do not apply to cover bi-directional charging equipment, or unidirectional power export equipment, covered by Annex A, Ref. No. 73B.

Categories: Electrical
Contact: [email protected] (Matthew Wong)
Origin: CSA
Close date: Jun 16, 2026
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1.1 This Standard applies to conductive electric vehicle (EV) supply equipment with a primary source voltage of 1000 V ac or less, with a frequency of 50 or 60 Hz, and intended to provide ac power to an electric vehicle with an on-board charging unit. This Standard covers electric vehicle supply equipment intended for use where ventilation is not required.

 

1.2 With reference to 1.1, the following list of examples of electric vehicle supply equipment are included in this Standard:

a) EV Cord Sets – Rated 125 Vac maximum, 16 A maximum, intended for indoor and outdoor use;

b) Fastened in place EV Charging Stations – Rated 250 Vac maximum, 40 A maximum, intended for indoor or outdoor use;

c) Fixed in place EV Charging Stations – Rated 1000 Vac maximum, intended for indoor or indoor/outdoor use; and

d) Fixed in place EV Power Outlet – Rated 1000 Vac maximum, intended for indoor or indoor/outdoor use.

For Mexico, use 127 Vac where 120 or 125 Vac is referenced in this Standard. In Canada and the United States, this does not apply.

 

1.3 The products covered by this Standard are intended for use in accordance with the Installation Codes in Annex A, Ref. No. 1.

 

1.4 This Standard does not cover cord sets or power supply cords for applications other than EV charging cord sets. For cord sets and power supply cords not covered by this Standard, refer to Annex A, Ref. No. 2 and No. 3.

 

1.5 With reference to 1.2, this Standard does not cover electric vehicle charging equipment. For EV charging equipment not covered by this Standard, refer to Annex A, Ref. No. 4.

 

1.6 This Standard does not cover electric vehicle connectors. For electric vehicle connectors not covered by this Standard, refer to Annex A, Ref. No. 5.

 

1.7 This Standard does not cover regular-use power outlets. For regular-use power outlets not covered by this Standard, refer to Annex A, Ref. No. 6.

 

1.8 This Standard does not cover equipment intended for wireless power transfer, which may also be designated as wireless charging, inductive charging, magnetic resonance charging, or any other similar designation indicating the transfer of power from the EVSE to the vehicle through other than a conductive connection.

 

1.9 This standard does not cover electric vehicle export equipment, allowing bi-directional current flow from the vehicle to off board loads. For electric vehicle power export equipment, refer to Annex A, Ref. No. 75.

Categories: Energy
Origin: CSA
Close date: Jun 19, 2026
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1.1 General

This Document specifies the key performance metrics, definitions, and evaluation steps necessary to assess the suitability of methane DMQ technologies for oil and gas applications. It applies to technologies used for detection, localisation, measurement, quantification, and reporting of methane emissions from components, equipment, or facilities. Providing a consistent reference framework for comparison and decision-making across technology types and deployment contexts. This Technical Specification applies to DMQ technology method classes defined by their operational characteristics and deployment platforms, including but not limited to:

a)    Handheld and portable devices;

b)   Emissions monitoring systems (EMS);

c)    Uncrewed aerial vehicles (UAVs);

d)   Satellite-based remote sensing systems;

e)    Vehicle-mounted or aircraft-based survey systems; and

f)    Parametric systems that utilize operational data to calculate emissions.

The framework addresses quantitative technology performance metrics that can be derived from technology-generated observations in comparison with reference measurements from controlled test facilities or validated field datasets.

It also includes qualitative performance considerations, such as environmental or situational variables, performance envelopes, and deployment factors, as specified by technology manufacturers or DMQ service providers.

This Document was developed with a focus on upstream, midstream, and downstream onshore oil and gas operations in Canada. Any specific limits on the types of infrastructure or emission sources to which this guidance applies will align with those defined in federal and provincial methane regulations (including Alberta, British Columbia, and Saskatchewan).

1.2 Inclusions

This technical specification applies to:

a)    Definitions and terminology relevant to methane DMQ technologies;

b)   A taxonomy of technology types and deployment contexts;

c)    Core performance metrics and validation parameters;

d)   A suggested evaluation process for technology selection and use case definition; and

e)    Reference materials and data sheet templates to support consistent documentation of results.

1.3 Exclusions

This technical specification does not:

a)    Provide detailed testing protocols for specific technology types or classes;

b)   Compare individual technology brands, models, or manufacturers;

c)    Describe or assess costs, ease of deployment, or training requirements, as such business considerations are beyond the scope of standardization; or

d)   Prescribe or list regulatory requirements, which remain the responsibility of the reader to identify and apply based on the jurisdiction and site type.

1.4 Terminology

In this technical specification, “shall” is used to express a requirement, i.e., a provision that the user is obliged to satisfy in order to comply with the technical specification; “should” is used to express a recommendation or that which is advised but not required; and “may” is used to express an option or that which is permissible within the limits of the technical specification.

Notes accompanying clauses do not include requirements or alternative requirements; the purpose of a note accompanying a clause is to separate from the text explanatory or informative material.

Notes to tables and figures are considered part of the table or figure and may be written as requirements.

Annexes are designated normative (mandatory) or informative (non-mandatory) to define their application.

Contact: [email protected] (Wesley Salifu)
Origin: CSA
Close date: Jun 23, 2026
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This document specifies general performance requirements for washer-disinfectors (WD) and washer-disinfector accessories that are intended to be used for cleaning and disinfection of reusable medical devices. It specifies performance requirements for cleaning and disinfection as well as for the accessories that can be required to achieve the necessary performance. The methods and instrumentation required for validation, routine control and monitoring and requalification, periodically and after essential repairs, are also specified.

NOTE 1 The requirements can be applied to WD intended for use with other articles used in the context of medical, dental, pharmaceutical and veterinary practice.

The requirements for WD intended to process specific loads are specified in ISO 15883-2ISO 15883-3ISO 15883-4ISO 15883-6 and ISO 15883-7. For WD intended to process loads of two or more different types, the requirements of the applicable parts of ISO 15883-2ISO 15883-3ISO 15883-4ISO 15883-6 and ISO 15883-7 apply.
This document does not specify requirements intended for machines for use for laundry or general catering purposes.
This document does not include requirements for machines which are intended to sterilize the load, or which are designated as “sterilizers” and addressed in other standards.
The specified performance requirements of this document do not ensure the inactivation or removal of the causative agent(s) (prion protein) of transmissible spongiform encephalopathies.

NOTE 2 Chemicals in some cleaning agents and disinfectants can react with prion protein in a manner that can inhibit its removal or inactivation.  If the presence of prion protein is considered a possibility, then this can influence the choice of cleaning agent and disinfectant.

NOTE 3 This document can be used by prospective purchasers and manufacturers as the basis of agreement on the specification of a WD. The test methods for demonstration of conformity with the requirements of this document can also be employed by users to demonstrate continued conformity of the installed WD throughout its service life. Guidance on a routine test programme is given in Annex A.