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CAN/CSA-ISO/IEC 14543-5-4-12
Information technology - Home electronic system (HES) architecture - Part 5-4: Intelligent grouping and resource sharing for HES Class 2 and Class 3 - Device validation
Edition
2012-03-01
CAN/CSA-ISO/IEC 18013-3
Information technology - Personal identification - ISO-compliant driving licence - Part 3: Access control, authentication and integrity validation (Adopted ISO/IEC 18013-3:2017, second edition, 2017-04)
Edition
2018-09-01
CAN/CSA-ISO/IEC 18013-3 AMD 1
Amendment 1:2022 to CAN/CSA-ISO/IEC 18013-3:18, Information technology - Personal identification - ISO-compliant driving licence - Part 3: Access control, authentication and integrity validation - Amendment 1: Pace protocol (Adopted amendment 1:2022 to ISO/IEC 18013-3:2017)
Edition
2021
CAN/CSA-ISO/IEC 19757-2-10
Information technology - Document Schema Definition Language (DSDL) - Part 2: Regular-grammar-based validation - RELAX NG
Edition
2010-12-01
CAN/CSA-ISO/IEC 19757-3
Information technology - Document Schema Definition Languages (DSDL) - Part 3: Rule-based validation - Schematron (Adopted ISO/IEC 19757-3:2016, second edition, 2016-01-15)
Edition
2018-01-01
CAN/CSA-ISO/IEC 19757-4-06
Information Technology - Document Schema Definition Languages (DSDL) - Part 4: Namespace-Based Validation Dispatching Language (NVDL)
Edition
2006-12-01
CAN/CSA-ISO 11137-3
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
CAN/CSA-ISO 14066-12
Greenhouse gases - Competence requirements for greenhouse gas validation teams and verification teams
Edition
2012-06-01
CAN/CSA-ISO 14937-11
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Edition
2011-10-01
CAN/CSA-Z11135
Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (Adopted ISO 11135:2014, second edition, 2014-07-15)
Edition
2015-11-01