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Notice of Intent
Standard for Categories 1 and 2 Foam Liquid Concentrates
1. The Standards for foam liquid concentrates are divided into three categories. Category 1 Primarily for use on general-purpose hydrocarbon fires Category 2 Primarily for use on polar solvents, oxygenated fuels, and water...
Committee
MC/IEC/TC 23/SC 23B
a) To prepare safety and performance standards for general purpose switches including electronic switches, for example, time-delay switches, remote control switches and isolating switches, with rated voltage not exceeding 440...
Committee
MC/ISO/TC 94/SC 14
ISO/TC 94/SC14 was established specifically to deal with the unique requirements for firefighters' Personal Protective Equipment (PPE). Under the scope of SC 14, each Standard for firefighters' PPE is developed for a...
Accreditation Bulletin
IAF MD 1:2023, Audit and Certification of a Management...
Action required All affected customers will be assessed against IAF MD 1:2023, Issue 3, IAF Mandatory Document for the Audit and Certification of a Management System Operated by a Multi-Site Organization at their next office...
Accreditation Bulletin
IAF MD 11:2023, Application of ISO/IEC 17021-...
Action required IAF MD 11:2023, Issue 3, IAF Mandatory Document for the Application of ISO/IEC 17021-1 for Audits of Integrated Management Systems (PDF) was issued in 2023. MSAP customers with integrated management systems...
Accreditation Bulletin
Withdrawal of SCC Requirements & Guidance on ...
Action required All references to the SCC Requirements & Guidance on the Use of Information Technology in Accredited Laboratories (RG Use of IT) should be removed from use. Affected customers All accredited and applicant...
Accreditation Bulletin
IAF MD23:2023 Control of Entities Operating on...
Action required IAF MD23:2023 Issue 2 Control of Entities Operating on Behalf of Accredited Management Systems Certification Bodies (PDF), was Issued on 20 December 2023, and is effective immediately. Affected customers All...
Notice of Intent
Canadian Medical Devices Reprocessing
This Standard addresses the safe, effective, and reliable reprocessing of reusable medical devices at each phase of the reprocessing workflow and it provides MDR specific requirements for QMS, personnel, MIFUs, purchase and...