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Complete Health Care Collection

SKU: 2700013 255 Documents Included

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Overview
Items Included

This collection of standards brings together CSA Group standards relating to health care facilities, medical labs, electromedical equipment, and electrical systems. These standards provide valuable guidance on the overall safety and efficiency of buildings, services, and systems, helping to protect both patients and healthcare professionals.

Used in the following areas/industries:

Infection prevention & control (IPC)
Healthcare facility planners
Architect and design firms (healthcare)
Construction managers
Contractors
Medical device manufacturers
Medical device reprocessing (MDR)

Ideal for the following roles:

Hospitals
Architects and Designers

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CSA ISO 17664-1:23

Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices (Adopted ISO 17664-1:2021, first edition, 2021-07)

Active

EnglishFrench

CSA C22.2 NO. 80601-2-67:23

Medical electrical equipment — Part 2-67: Particular requirements for basic safety and essential performance of oxygen conserving equipment (Adopted ISO 80601-2-67:2020, second edition, 20204-10, with Canadian deviations)

Active

EnglishFrench

CSA C22.2 NO. 80601-2-74:23

Medical electrical equipment — Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment (Adopted ISO 80601-2-74:2021, second edition, 2021-07, with Canadian deviations)

Active

EnglishFrench

CSA ISO 15883-5:23

Washer-disinfectors — Part 5: Performance requirements and test method criteria for demonstrating cleaning efficacy (Adopted ISO 15883-5:2021, first edition, 2021-07)

Active

EnglishFrench

CSA Z364.6:23

Quality management for kidney dialysis providers

Active

EnglishFrench

CSA ISO/TS 16775:23

Packaging for terminally sterilized medical devices — Guidance on the application of ISO 11607-1 and ISO 11607-2 (Adopted ISO Technical Specification 16775:2021, second edition, 2021-11)

Active

EnglishFrench

CSA Z314:23

Canadian medical device reprocessing in all health care settings

Active

EnglishFrench

CSA ISO 17664-2:23

Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices (Adopted ISO 17664-2:2021, first edition, 2021-02)

Active

EnglishFrench

CSA/ASC B652:23

Accessible dwellings

Active

EnglishFrench

CSA C22.2 NO. 80601-2-70:23

Medical electrical equipment — Part 2-70: Particular requirements for the basic safety and essential performance of sleep apnoea breathing therapy equipment (Adopted ISO 80601-2-70:2020, second edition, 2020-11, with Canadian deviations)

Active

EnglishFrench

CAN/CSA-Z900.2.3:22

Perfusable organs for transplantation

Active

EnglishFrench

CAN/CSA-Z900.2.4:22

Ocular tissues for transplantation

Active

EnglishFrench

CAN/CSA-Z900.2.5:22

Lymphohematopoietic cells for transplantation

Active

EnglishFrench

CAN/CSA-Z900.2.2:22

Tissues for transplantation

Active

EnglishFrench

CSA Z317.13:22

Infection control during construction, renovation, and maintenance of health care facilities

Active

EnglishFrench

CSA Z7396.1:22

Medical gas pipeline systems - Part 1: Pipelines for medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems

Active

EnglishFrench

CSA Z364.5:22

Safe installation and operation of haemodialysis and peritoneal dialysis in a home setting

Active

EnglishFrench

CSA Z1635:22

Functional requirements and core data set for a Canadian paramedic information system (CPIS)

Active

EnglishFrench

CSA ISO 20166-1:22

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 1: Isolated RNA (Adopted ISO 20166-1:2018, first edition, 2018-12)

Active

EnglishFrench

CSA ISO 20166-2:22

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 2: Isolated proteins (Adopted ISO 20166-2:2018, first edition, 2018-12)

Active

EnglishFrench

CSA ISO 20166-3:22

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 3: Isolated DNA (Adopted ISO 20166-3:2018, first edition, 2018-12)

Active

EnglishFrench

CSA ISO 20166-4:22

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 4: In situ detection techniques (Adopted ISO 20166-4:2021, first edition, 2021-07)

Active

EnglishFrench

CSA ISO 20186-1:22

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA (Adopted ISO 20186-1:2019, first edition, 2019-02)

Active

EnglishFrench

CSA ISO 20186-2:22

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA (Adopted ISO 20186-2:2019, first edition, 2019-02)

Active

EnglishFrench

CSA ISO 20186-3:22

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma (Adopted ISO 20186-3:2019, first edition, 2019-09)

Active

EnglishFrench

CSA Z8004:22

Long-term care home operations and infection prevention and control

Active

EnglishFrench

CAN/CSA-Z900.1:22

Cells, tissues, and organs for transplantation: General requirements

Active

EnglishFrench

CSA Z317.10:21

Handling of health care waste materials

Active

English

CSA ISO 15190:21

Medical laboratories - Requirements for safety (Adopted ISO 15190:2020, second edition, 2020-02)

Active

English

CSA ISO/TS 11137-4:21

Sterilization of health care products — Radiation — Part 4: Guidance on process control (Adopted ISO technical specification 11137-4:2020, first edition, 2020-06)

Active

English

CSA C22.2 NO. 80601-2-84:21

Medical electrical equipment — Part 2-84: Particular requirements for the basic safety and essential performance of ventilators for the emergency medical services environment (Adopted ISO 80601-2-84:2020, first edition, 2020-07, with Canadian deviations)

Active

EnglishFrench

CSA Z76.1:21

Reclosable child-resistant packages

Active

EnglishFrench

CSA ISO 14971:21

Medical devices – Application of risk management to medical devices (Adopted ISO 14971:2019, third edition, 2019-12)

Active

EnglishFrench

CSA Z32:21

Electrical safety and essential electrical systems in health care facilities

Active

EnglishFrench

CSA Z11138-7:21

Sterilization of health care products — Biological indicators — Part 7: Guidance for the selection, use and interpretation of results (Adopted ISO 11138-7:2019, with Canadian deviations)

Active

EnglishFrench

CSA ISO 8637-1:21

Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (Adopted ISO 8637-1:2017, first edition, 2017-11)

Active

EnglishFrench

CSA ISO 8637-2:21

Extracorporeal systems for blood purification — Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (Adopted ISO 8637-2:2018, first edition, 2018-07)

Active

EnglishFrench

CSA ISO 11607-2:21

Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes (Adopted ISO 11607-2:2019, second edition, 2019-02)

Active

EnglishFrench

CSA ISO 11607-1:21

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems (Adopted ISO 11607-1:2019, second edition, 2019-02)

Active

EnglishFrench

CSA Z1650:21

Paramedic response to the opioid crisis: Education and training across the treatment and care continuum in out-of-hospital and community settings

Active

EnglishFrench

CSA ISO 11737-2:21

Sterilization of health care products — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (Adopted ISO 11737-2:2019, third edition, 2019-12)

Active

EnglishFrench

CSA ISO 22367:21

Medical laboratories — Application of risk management to medical laboratories (Adopted ISO 22367:2020, first edition, 2020-02)

Active

EnglishFrench

CSA Z8003:21

Health care facility design studies and post-occupancy evaluation

Active

EnglishFrench

CSA ISO/TR 24971:21

Medical devices — Guidance on the application of ISO 14971 (Adopted ISO/TR 24971:2020, second edition, 2020-06)

Active

EnglishFrench

CSA Z317.1:21

Special requirements for plumbing installations in health care facilities

Active

EnglishFrench

CSA Z325:20

Hip protectors

Active

English

CSA Z316.6:20

Sharps injury protection - Requirements and test methods - Sharps containers (Adopted ISO 23907-2:2019, first edition, 2019-11, with Canadian deviations)

Active

EnglishFrench

CSA Z386:20

Safe use of lasers in health care

Active

EnglishFrench

CAN/CSA-Z902:20

Blood and blood components

Active

EnglishFrench

CSA Z316.5:20

Fume hoods and associated exhaust systems

Active

EnglishFrench

CSA Z23500-4:20

Preparation and quality management of fluids for haemodialysis and related therapies —Part 4: Concentrates for haemodialysis and related therapies (Adopted ISO 23500-4:2019, first edition, 2019-02, with Canadian deviations)

Active

EnglishFrench

CSA Z23500-3:20

Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies (Adopted ISO 23500-3:2019, first edition, 2019-02, with Canadian deviations)

Active

EnglishFrench

CSA Z23500-5:20

Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapies (Adopted ISO 23500-5:2019, first edition, 2019-02, with Canadian deviations)

Active

EnglishFrench

CSA Z23500-2:20

Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapies (Adopted ISO 23500-2:2019, first edition, 2019-02, with Canadian deviations)

Active

EnglishFrench

CSA Z23500-1:20

Preparation and quality management of fluids for haemodialysis and related therapies — Part 1: General requirements (Adopted ISO 23500-1: 2019, first edition, 2019-02, with Canadian deviations)

Active

EnglishFrench

CSA ISO/TS 20914:20

Medical laboratories — Practice guidance for the estimation of measurement uncertainty (Adopted ISO technical specification 20914:2019, first edition, 2019-07)

Active

EnglishFrench

CSA Z317.12:20

Cleaning and disinfection of health care facilities

Active

EnglishFrench

CSA Z16686:20

Osteopathic healthcare provision (Adopted CEN EN 16686:2015, first edition, 2015-07, with Canadian deviations)

Active

EnglishFrench

CSA Z2003:20

Mental health and well-being for post-secondary students

Active

EnglishFrench

CSA ISO 8836:20

Suction catheters for use in the respiratory tract (Adopted ISO 8836:2019, fifth edition, 2019-12)

Active

EnglishFrench

CSA ISO 11195:19

Gas mixers for medical use - Stand-alone gas mixers (Adopted ISO 11195:2018, second edition, 2018-01)

Active

English

CSA ISO/TR 13154:19

Medical electrical equipment — Deployment, implementation and operational guidelines for identifying febrile humans using a screening thermograph (Adopted ISO/TR 13154:2017, second edition, 2017-03)

Active

English

CSA ISO 18835:19

Inhalational anaesthesia systems — Draw-over anaesthetic systems (Adopted ISO 18835:2015, first edition, 2015-04-01)

Active

English

CSA Z317.2:19

Special requirements for heating, ventilation, and air-conditioning (HVAC) systems in health care facilities

Active

EnglishFrench

CSA Z10524-1:19

Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (Adopted ISO 10524-1:2018, second edition, 2018-01, with Canadian deviations)

Active

EnglishFrench

CSA ISO 15883-4:19

Washer-disinfectors — Part 4: Requirements and tests for washer-disinfectors employing chemical disinfection for thermolabile endoscopes (Adopted ISO 15883-4:2018, second edition, 2018-11)

Active

EnglishFrench

CSA Z10524-3:19

Pressure regulators for use with medical gases - Part 3: Pressure regulators integrated with cylinder valves (Adopted ISO 10524-3:2019, second edition, 2019-01, with Canadian deviations)

Active

EnglishFrench

CSA Z10524-2:19

Pressure regulators for use with medical gases - Part 2: Manifold and line pressure regulators (Adopted ISO 10524-2:2018, second edition, 2018-01, with Canadian deviations)

Active

EnglishFrench

CSA Z387:19

Safe use of electrosurgical medical devices and systems in health care

Active

EnglishFrench

CSA Z8002:19

Operation and maintenance of health care facilities

Active

EnglishFrench

CSA ISO 5367:19

Anaesthetic and respiratory equipment — Breathing sets and connectors (Adopted ISO 5367:2014, fifth edition, 2014-10-15)

Active

EnglishFrench

CSA ISO 81060-2:19

Non-invasive sphygmomanometers - Part 2: Clinical investigation of automated measurement type (Adopted ISO 81060-2:2018, third edition, 2018-11)

Active

EnglishFrench

CSA ISO 11139:19

Sterilization of health care products — Vocabulary of terms used in sterilization and related equipment and process standards (Adopted ISO 11139:2018, first edition, 202018-08)

Active

EnglishFrench

CSA ISO 20857:19

Sterilization of health care products — Dry heat — Requirements for the development, validation and routine control of a sterilization process for medical devices (Adopted ISO 20857:2010, first edition, 2010-08-15

Active

EnglishFrench

CSA ISO 11737-1:19

Sterilization of health care products — Microbiological methods — Part 1: Determination of a population of microorganisms on products (Adopted ISO 11737-1:2018, third edition, 2018-01)

Active

EnglishFrench

CSA ISO 19223:19

Lung ventilators and related equipment — Vocabulary and semantics (Adopted ISO 19223:2019, first edition, 2019-07)

Active

EnglishFrench

CSA Z630:19

Barbecue grill brushes

Active

EnglishFrench

CSA Z9170-1:19

Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases, vacuum, and anaesthetic gas scavenging systems (Adopted ISO 9170-1:2017, third edition, 2017-07, with Canadian deviations)

Active

EnglishFrench

CAN/CSA-ISO 11140-4:18 (R2023)

Sterilization of health care products — Chemical indicators — Part 4: Class 2 indicators as an alternative to the Bowie and Dick-type test for detection of steam penetration (Adopted ISO 11140-4:2007, second edition, 2007-03-15)

Active

English

CAN/CSA-ISO 5356-2:18

Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors (Adopted ISO 5356-2:2012, third edition, 2012-11-15)

Active

EnglishFrench

CAN/CSA-Z23747:18

Anaesthetic and respiratory equipment - Peak expiratory flow meters for the assessment of pulmonary function in spontaneously breathing humans (Adopted ISO 23747:2015, second edition, 2015-08-01, with Canadian deviations)

Active

EnglishFrench

Z8000-18

Canadian health care facilities

Active

EnglishFrench

CAN/CSA-ISO 5366:18

Anaesthetic and respiratory equipment — Tracheostomy tubes and connectors (Adopted ISO 5366:2016, first edition, 2016-10-01)

Active

EnglishFrench

Z7000-18 (R2023)

General requirements for quality management and safety in perioperative settings

Active

EnglishFrench

CSA Z316.8:18 (R2023)

Requirements for the design, development, and validation of laboratory-developed tests used for the screening, diagnosis, and management of clinical conditions

Active

EnglishFrench

CAN/CSA-ISO 11140-3:18 (R2023)

Sterilization of health care products — Chemical indicators — Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test (Adopted ISO 11140-3:2007, second edition, 2007-03-15, including technical corrigendum 1:2007)

Active

EnglishFrench

CAN/CSA-ISO 11140-5:18 (R2023)

Sterilization of health care products — Chemical indicators — Part 5: Class 2 indicators for Bowie and Dick-type air removal tests (Adopted ISO 11140-5:2007, second edition, 2007-03-15)

Active

EnglishFrench

CAN/CSA-ISO 5361:18

Anaesthetic and respiratory equipment — Tracheal tubes and connectors (Adopted ISO 5361:2016, third edition, 2016-09-01)

Active

EnglishFrench

CAN/CSA-ISO IWA 18:17 (R2022)

Framework for integrated community-based life-long health and care services in aged societies (Adopted ISO International Workshop Agreement 18:2016, first edition, 2016-06-15)

Active

English

CAN/CSA-ISO/TS 17665-3:17 (R2022)

Sterilization of health care products — Moist heat — Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization (Adopted ISO/TS 17665-3:2013, first edition, 2013-04-15)

Active

English

CSA C22.2 NO. 80601-2-72:17 (R2022)

Medical electrical equipment — Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients (Adopted ISO 80601-2-72:2015, first edition, 2015-09-01, with Canadian deviations)

Active

EnglishFrench

CSA Z317.11:17 (R2022)

Area measurement for health care facilities

Active

EnglishFrench

CAN/CSA-Z900.2.1-17 (R2022)

Tissues for assisted reproduction

Active

EnglishFrench

CAN/CSA-ISO 11137-3:17 (R2022)

Sterilization of health care products — Radiation — Part 3: Guidance on dosimetric aspects of development, validation and routine control (Adopted ISO 11137-3:2017, second edition, 2017-06)

Active

EnglishFrench

CAN/CSA-ISO 11138-1:17 (R2022)

Sterilization of health care products — Biological indicators — Part 1: General requirements (Adopted ISO 11138-1:2017, third edition, 2017-03)

Active

EnglishFrench

CSA Z10535.2:17 (R2022)

Lifts for the transfer of persons - Installation, use, and maintenance

Active

EnglishFrench

CSA Z317.14:17 (R2022)

Wayfinding for health care facilities

Active

EnglishFrench

CAN/CSA-Z1630-17 (R2022)

Community paramedicine: Framework for program development

Active

EnglishFrench

CAN/CSA-ISO 11138-4:17 (R2022)

Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization (Adopted ISO 11138-4:2017, second edition, 2017-03)

Active

EnglishFrench

CAN/CSA-ISO 11138-3:17 (R2022)

Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processes (Adopted ISO 11138-3:2017, third edition, 2017-03)

Active

EnglishFrench

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Complete Health Care Collection

Product Details

Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices (Adopted ISO 17664-1:2021, first edition, 2021-07)

Medical electrical equipment — Part 2-67: Particular requirements for basic safety and essential performance of oxygen conserving equipment (Adopted ISO 80601-2-67:2020, second edition, 20204-10, with Canadian deviations)

Medical electrical equipment — Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment (Adopted ISO 80601-2-74:2021, second edition, 2021-07, with Canadian deviations)

Washer-disinfectors — Part 5: Performance requirements and test method criteria for demonstrating cleaning efficacy (Adopted ISO 15883-5:2021, first edition, 2021-07)

Quality management for kidney dialysis providers

Packaging for terminally sterilized medical devices — Guidance on the application of ISO 11607-1 and ISO 11607-2 (Adopted ISO Technical Specification 16775:2021, second edition, 2021-11)

Canadian medical device reprocessing in all health care settings

Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices (Adopted ISO 17664-2:2021, first edition, 2021-02)

Accessible dwellings

Medical electrical equipment — Part 2-70: Particular requirements for the basic safety and essential performance of sleep apnoea breathing therapy equipment (Adopted ISO 80601-2-70:2020, second edition, 2020-11, with Canadian deviations)

Perfusable organs for transplantation

Ocular tissues for transplantation

Lymphohematopoietic cells for transplantation

Tissues for transplantation

Infection control during construction, renovation, and maintenance of health care facilities

Medical gas pipeline systems - Part 1: Pipelines for medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems

Safe installation and operation of haemodialysis and peritoneal dialysis in a home setting

Functional requirements and core data set for a Canadian paramedic information system (CPIS)

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 1: Isolated RNA (Adopted ISO 20166-1:2018, first edition, 2018-12)

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 2: Isolated proteins (Adopted ISO 20166-2:2018, first edition, 2018-12)

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 3: Isolated DNA (Adopted ISO 20166-3:2018, first edition, 2018-12)

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 4: In situ detection techniques (Adopted ISO 20166-4:2021, first edition, 2021-07)

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA (Adopted ISO 20186-1:2019, first edition, 2019-02)

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA (Adopted ISO 20186-2:2019, first edition, 2019-02)

Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma (Adopted ISO 20186-3:2019, first edition, 2019-09)

Long-term care home operations and infection prevention and control

Cells, tissues, and organs for transplantation: General requirements

Handling of health care waste materials

Medical laboratories - Requirements for safety (Adopted ISO 15190:2020, second edition, 2020-02)

Sterilization of health care products — Radiation — Part 4: Guidance on process control (Adopted ISO technical specification 11137-4:2020, first edition, 2020-06)

Medical electrical equipment — Part 2-84: Particular requirements for the basic safety and essential performance of ventilators for the emergency medical services environment (Adopted ISO 80601-2-84:2020, first edition, 2020-07, with Canadian deviations)

Reclosable child-resistant packages

Medical devices – Application of risk management to medical devices (Adopted ISO 14971:2019, third edition, 2019-12)

Electrical safety and essential electrical systems in health care facilities

Sterilization of health care products — Biological indicators — Part 7: Guidance for the selection, use and interpretation of results (Adopted ISO 11138-7:2019, with Canadian deviations)

Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (Adopted ISO 8637-1:2017, first edition, 2017-11)

Extracorporeal systems for blood purification — Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (Adopted ISO 8637-2:2018, first edition, 2018-07)

Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes (Adopted ISO 11607-2:2019, second edition, 2019-02)

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems (Adopted ISO 11607-1:2019, second edition, 2019-02)

Paramedic response to the opioid crisis: Education and training across the treatment and care continuum in out-of-hospital and community settings

Sterilization of health care products — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (Adopted ISO 11737-2:2019, third edition, 2019-12)

Medical laboratories — Application of risk management to medical laboratories (Adopted ISO 22367:2020, first edition, 2020-02)

Health care facility design studies and post-occupancy evaluation

Medical devices — Guidance on the application of ISO 14971 (Adopted ISO/TR 24971:2020, second edition, 2020-06)

Special requirements for plumbing installations in health care facilities

Hip protectors

Sharps injury protection - Requirements and test methods - Sharps containers (Adopted ISO 23907-2:2019, first edition, 2019-11, with Canadian deviations)

Safe use of lasers in health care

Blood and blood components

Fume hoods and associated exhaust systems

Preparation and quality management of fluids for haemodialysis and related therapies —Part 4: Concentrates for haemodialysis and related therapies (Adopted ISO 23500-4:2019, first edition, 2019-02, with Canadian deviations)

Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies (Adopted ISO 23500-3:2019, first edition, 2019-02, with Canadian deviations)

Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapies (Adopted ISO 23500-5:2019, first edition, 2019-02, with Canadian deviations)

Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapies (Adopted ISO 23500-2:2019, first edition, 2019-02, with Canadian deviations)

Preparation and quality management of fluids for haemodialysis and related therapies — Part 1: General requirements (Adopted ISO 23500-1: 2019, first edition, 2019-02, with Canadian deviations)

Medical laboratories — Practice guidance for the estimation of measurement uncertainty (Adopted ISO technical specification 20914:2019, first edition, 2019-07)

Cleaning and disinfection of health care facilities

Osteopathic healthcare provision (Adopted CEN EN 16686:2015, first edition, 2015-07, with Canadian deviations)

Mental health and well-being for post-secondary students