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Scope This part of ISO/IEC 15408 defines the assurance requirements of ISO/IEC 15408. It includes the evaluation assurance levels (EALs) that define a scale for measuring assurance for component TOEs, the composed assurance...

Scope This part of ISO/IEC 15408 defines the required structure and content of security functional components for the purpose of security evaluation. It includes a catalogue of functional components that will meet the common...

Scope This part of ISO/IEC 11694 specifies the logical data structures for optical memory cards necessary to allow compatibility and interchange between systems using the linear recording method.

Scope This part of ISO/IEC 8632 specifies a binary encoding of the Computer Graphics Metafile. For each of the elements specified in ISO/IEC 8632-1, this part specifies an encoding in terms of data types. For each of these...

This part of ISO/IEC 10118 specifies dedicated hash-functions, i.e. specially designed hash-functions. The hash-functions in this part of ISO/IEC 10118 are based on the iterative use of a round-function. Seven distinct round...

This part of ISO/IEC 9314 specifies a series of tests in order to verify conformance of FDDI stations to the requirements of ISO/IEC 9314-3:1990. NOTE: ISO/IEC 9314-3 specifies the requirements for the optical input/output...

This part of ISO/IEC 13719 defines the binding of the Portable Common Tool Environment (PCTE), as specified in ISO/IEC 13719-1, to the C programming language. A number of features are not completely defined in ISO/IEC 13719-1...

specifies requirements and provides guidance on the enumeration and microbial characterization of the population of viable microorganisms on or in a health care product, component, raw material or package

specifies general performance requirements for washer-disinfectors (WD) and their accessories that are intended to be used for cleaning and disinfection of re-usable medical devices and other articles used in the context of...

specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices. It also specifies requirements and provides guidance in relation to depyrogenation processes...

ISO 10524-1:2018 specifies the design, construction, type testing, and marking requirements for pressure regulators intended for the administration of medical gases and their mixtures in the treatment, management, diagnostic...

ISO 10524-2:2018 specifies design, construction, type testing, and marking requirements for manifold pressure regulators and line pressure regulators intended for use in medical gas pipeline systems. Examples of gases include...