This list of COVID-19 resources has been compiled by the International Organization for Standardization to support global efforts in dealing with the crisis. They are freely available in a read-only format:
- ISO 374-5:2016, “Protective gloves against dangerous chemicals and micro-organisms—Part 5: Terminology and performance requirements for micro-organisms risk”
- ISO 10651-3:1997, “Lung ventilators for medical use—Part 3: Particular requirements for emergency and transport ventilators”
- ISO 10651-4:2002, “Lung ventilators—Part 4: Particular requirements for operator-powered resuscitators”
- ISO 10651-5:2006, “Lung ventilators for medical use—Particular requirements for basic safety and essential performance — Part 5: Gas-powered emergency resuscitators”
- ISO 10993-1:2018, “Biological evaluation of medical devices—Part 1: Evaluation and testing within a risk management process”
- ISO 13485:2016, “Medical devices—Quality management systems—Requirements for regulatory purposes”
- ISO 13688:2013, “Protective clothing—General requirements”
- ISO 17510:2015, “Medical devices—Sleep apnoea breathing therapy—Masks and application accessories”
- ISO 18082:2014, “Anaesthetic and respiratory equipment—Dimensions of non-interchangeable screw-threaded (NIST) low-pressure connectors for medical gases” [Including ISO 18082:2014/AMD 1:2017, AMENDMENT 1]
- ISO 18562-1:2017, “Biocompatibility evaluation of breathing gas pathways in healthcare applications—Part 1: Evaluation and testing within a risk management process”
- ISO 18562-2:2017, “Biocompatibility evaluation of breathing gas pathways in healthcare applications—Part 2: Tests for emissions of particulate matter”
- ISO 18562-3:2017, “Biocompatibility evaluation of breathing gas pathways in healthcare applications—Part 3: Tests for emissions of volatile organic compounds (VOCs)”
- ISO 18562-4:2017, “Biocompatibility evaluation of breathing gas pathways in healthcare applications—Part 4: Tests for leachables in condensate”
- ISO 19223:2019, “Lung ventilators and related equipment—Vocabulary and semantics”
- ISO 20395:2019, “Biotechnology—Requirements for evaluating the performance of quantification methods for nucleic acid target sequences—qPCR and dPCR”
- ISO 22301:2019, “Security and resilience—Business continuity management systems—Requirements”
- ISO 22395:2018, “Security and resilience—Community resilience—Guidelines for supporting vulnerable persons in an emergency”
- ISO 22320:2018, “Security and resilience—Emergency management—Guidelines for incident management”
- ISO 22316:2017, “Security and resilience—Organizational resilience—Principles and attributes
- ISO 31000:2018, “Risk management—Guidelines”
- ISO 5356-1:2015, “Anaesthetic and respiratory equipment—Conical connectors—Part 1: Cones and sockets”
- ISO 80601-2-12:2020, “Medical electrical equipment—Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators”
- ISO 80601-2-13:2011, “Medical electrical equipment—Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation” [Including: ISO 80601-2-13:2011/Amd.1:2015, AMENDMENT 1 and ISO 80601-2-13:2011/Amd.2:2018, AMENDMENT 2]
- ISO 80601-2-70:2015, “Medical electrical equipment—Part 2-70: Particular requirements for basic safety and essential performance of sleep apnoea breathing therapy equipment”
- ISO 80601-2-74:2017, “Medical electrical equipment—Part 2-74: Particular requirements for basic safety and essential performance of respiratory humidifying equipment”
- ISO 80601-2-79:2018, “Medical electrical equipment—Part 2-79: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory impairment”
- ISO 80601-2-80:2018, “Medical electrical equipment—Part 2-80: Particular requirements for basic safety and essential performance of ventilatory support equipment for ventilatory insufficiency”
- ISO/TS 16976-8:2013, “Respiratory protective devices—Human factors—Part 8: Ergonomic factors”