Search

1.1 * Purpose This standard defines the life cycle requirements for MEDICAL DEVICE SOFTWARE. The set of PROCESSES, ACTIVITIES, and TASKS described in this standard establishes a common framework for MEDICAL DEVICE SOFTWARE...

1 Scope 1.1 These requirements cover electrical energy storage assemblies such as battery packs and combination battery pack-electrochemical capacitor assemblies and the subassembly/modules that make up these assemblies for...

Note: The scope for this NOI (originally published on May 30, 2023) was updated by the responsible SDO on November 19, 202 4. 1.1 Inclusions This Standard defines minimum energy efficiency and performance requirements for LED...

The purpose of key management is to provide procedures for handling cryptographic keying material to be used in symmetric or asymmetric cryptographic algorithms according to the security policy in force. This part of ISO/IEC...

This Standard specifies the technical requirements for the licensee to ensure structural integrity of cold-worked Zr-2.5 wt% Nb alloy pressure tubes in operating CANDU reactors. Clause 13 of CSA N285.0/N285.6 Series requires...

This part of ISO/IEC 16500 provides a toolbox consisting of lower layer protocols and physical interfaces. Each tool is applicable at one or more of the reference points within the delivery system. The physical delivery media...

.1 This Standard applies to supplementary protectors of the manual-reset type that may or may not have a manual means of operation and are intended for use as components within appliances or other electrical equipment where...

1 Scope This International Standard specifies the Systems Security Engineering – Capability Maturity Model® (SSE-CMM®). The SSE-CMM® is a process reference model focused upon the requirements for implementing security in a...

1.1 Except as indicated in Clause 1.2, Part 1 of this Standard applies to all boilers, pressure vessels, pressure piping, and fittings, as provided for by the Act (as defined in Clause 3) and identified in Part 1 of this...

1.1 This Standard specifies the technical requirements for the interconnection of distributed resources (DR) and distribution systems up to 50 kV line to line. This Standard covers all distributed resource technologies with...

.1 This part of ISO 9170 applies to: a) terminal units intended for use in medical gas pipeline systems in accordance with ISO 7396-1, for use with the following medical gases: - oxygen; - nitrous oxide; - medical air; -...

The CDIF family of standards is primarily designed to be used as a description of a mechanism for transferring information between modelling tools. It facilitates a successful transfer when the authors of the importing and...