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Complete Health Care Collection
Product Details
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
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)
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)
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)
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)
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)
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)
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)
CSA Z317.13:22
Infection control during construction, renovation, and maintenance of health care facilities
CSA Z7396.1:22
Medical gas pipeline systems - Part 1: Pipelines for medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems
CSA Z364.5:22
Safe installation and operation of haemodialysis and peritoneal dialysis in a home setting
CSA Z1635:22
Functional requirements and core data set for a Canadian paramedic information system (CPIS)
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)
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)