Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems (Adopted IEC 60601-1-8:2006, edition 2:2006 consolidated with amendment 1:2012 and amendment 2:2020, with Canadian deviations)
Edition 2022-08-01

Information technology - Service management - Part 12: Guidance on the relationship between ISO/IEC 20000-1:2011 and service management frameworks: CMMI-SVC (Adopted ISO/IEC TR 20000-12:2016, first edition, 2016-10-01)
Edition 2018-01-01

Governance of information technology - Guidance for principles-based standards in the governance of information technology (Adopted ISO/IEC TR 38504:2016, first edition, 2016-09-15)
Edition 2018-01-01

Information technology - Security techniques - Information security management systems - Guidance (Adopted ISO/IEC 27003:2017, second edition, 2017-03)
Edition 2018-09-01

Information technology - Security techniques - Guidance on assuring suitability and adequacy of incident investigative method (Adopted ISO/IEC 27041:2015, first edition, 2015-06-15)
Edition 2018-09-01

Systems and software engineering - Information technology project performance benchmarking framework - Part 3: Guidance for reporting (Adopted ISO/IEC 29155-3:2015, first edition, 2015-11-15)
Edition 2016-12-01

Systems and software engineering - Information technology project performance benchmarking framework - Part 4: Guidance for data collection and maintenance (Adopted ISO/IEC 29155-4:2016, first edition, 2016-10-15)
Edition 2018-01-01

Information technology - User interfaces - Voice commands - Part 1: Framework and general guidance (Adopted ISO/IEC 30122-1:2016, first edition, 2016-08-01)
Edition 2018-01-01

Ergonomics of human-system interaction - Part 171: Guidance on software accessibility (Adopted ISO 9241-171:2008, first edition, 2008-07-15)
Edition 2014-03-01

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)
Edition 2017-08-01